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-{"question": "Gene AGTR2 has a genetic association with diseases such as", "references": ["cystic fibrosis", "CF", "mucoviscidosis", "CYSTIC FIBROSIS", "CYSTIC FIBROSIS; CF"]}
-{"question": "Gene Generalized pustular psoriasis has a genetic association with diseases such as", "references": ["IL36RN", "FIL1", "FIL1(DELTA)", "FIL1D", "IL1F5", "IL1HY1", "IL1L1", "IL1RP3", "IL36RA", "PSORP", "IL-36Ra", "PSORS14", "interleukin 36 receptor antagonist"]}
-{"question": "Gene TMOD1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene KCNT1 has a genetic association with diseases such as", "references": ["Epilepsy in children", "Childhood seizure"]}
-{"question": "Gene Laurence-Moon syndrome has a genetic association with diseases such as", "references": ["PNPLA6", "BNHS", "NTE", "NTEMND", "SPG39", "iPLA2delta", "sws", "LNMS", "OMCS", "patatin like phospholipase domain containing 6"]}
-{"question": "Gene Omenn syndrome has a genetic association with diseases such as", "references": ["RAG1", "RAG-1", "RNF74", "recombination activating gene 1", "recombination activating 1", "RAG2", "RAG-2", "recombination activating gene 2", "recombination activating 2", "DCLRE1C", "A-SCID", "DCLREC1C", "RS-SCID", "SCIDA", "SNM1C", "DNA cross-link repair 1C"]}
-{"question": "Gene KCNJ8 has a genetic association with diseases such as", "references": ["Cant\u00fa syndrome", "hypertrichotic osteochondrodysplasia Cantu type", "Cantu syndrome", "Hypertrichotic osteochondrodysplasia, Cantu type", "Craniofaciocardioskeletal syndrome", "Hypertrichotic osteochondrodysplasia"]}
-{"question": "Gene muscle-eye-brain disease has a genetic association with diseases such as", "references": ["LARGE1", "MDC1D", "MDDGA6", "MDDGB6", "LARGE", "like-glycosyltransferase", "LARGE xylosyl- and glucuronyltransferase 1", "B3GALNT2", "B3GalNAc-T2", "MDDGA11", "beta-1,3-N-acetylgalactosaminyltransferase 2"]}
-{"question": "Gene Brunner Syndrome has a genetic association with diseases such as", "references": ["MAOA", "MAO-A", "monoamine oxidase A", "BRNRS"]}
-{"question": "Gene INVS has a genetic association with diseases such as", "references": ["gestational hypertension", "hypertension induced by pregnancy", "pregnancy associated hypertension", "pregnancy toxemia", "Pregnancy-induced hypertension", "hypertension-associated pregnancy disorder", "Hypertension Associated Disorders of Pregnancy", "Hypertension-Associated Pregnancy Disorder", "pre-eclampsia", "Pre-eclampsia, preeclampsia", "Pre-eclampsia or eclampsia superimposed on pre-existing hypertension", "pregnancy associated hypertension", "preeclampsia/eclampsia", "toxaemia of pregnancy", "hypertension induced by pregnancy", "gestational hypertension", "proteinuric hypertension of pregnancy", "pregnancy toxemia", "pre-eclamptic toxaemia", "preeclampsia", "Pre-eclampsia"]}
-{"question": "Gene Borjeson-Forssman-Lehmann syndrome has a genetic association with diseases such as", "references": ["PHF6", "BFLS", "BORJ", "CENP-31", "PHD finger protein 6"]}
-{"question": "Gene ASRGL1 has a genetic association with diseases such as", "references": ["chronic obstructive pulmonary disease", "COPD", "chronic obstructive airway disease", "chronic obstructive airways disease NOS", "chronic obstructive lung disease", "chronic obstructive airways disease NOS disorder", "chronic obstructive lung disease disorder", "COLD", "COLD (chronic obstructive lung disease)", "Chronic Obstructive Pulmonary Disease, (COPD)", "Pulmonary Disease (COPD), Chronic Obstructive", "Obstructive Pulmonary Disease (COPD), Chronic", "Chronic Obstructive Airways Disease", "Disease (COPD), Chronic Obstructive", "Chronic Obstructive Pulmonary Disease (COPD)", "obstructive lung disease, chronic", "COPD, Chronic Obstructive Pulmonary Disease", "Pulmonary Disease, Chronic Obstructive"]}
-{"question": "Gene LHPP has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene frontotemporal lobar degeneration has a genetic association with diseases such as", "references": ["PSEN1", "Psen1", "Ad3h", "PS-1", "PS1", "S182", "AD3", "FAD", "presenilin 1", "ACNINV3"]}
-{"question": "Gene POU3F4 has a genetic association with diseases such as", "references": ["nonsyndromic deafness", "nonsyndromic hearing loss", "nonsyndromic hereditary hearing loss", "Familial deafness", "Non-syndromic genetic deafness", "Isolated genetic deafness"]}
-{"question": "Gene neuromuscular disease has a genetic association with diseases such as", "references": ["TRPV4", "BCYM3", "CMT2C", "HMSN2C", "OTRPC4", "SMAL", "SPSMA", "SSQTL1", "TRP12", "VRL2", "VROAC", "transient receptor potential cation channel subfamily V member 4"]}
-{"question": "Gene PPARG has a genetic association with diseases such as", "references": ["type 2 diabetes", "NIDDM", "non-insulin-dependent diabetes mellitus", "type II diabetes mellitus", "Diabetes mellitus type 2", "Rare insulin-independent diabetes mellitus", "Diabetes Mellitus, Type 2", "type 2 diabetes mellitus", "diabetes (type 2)", "familial partial lipodystrophy", "Dunnigan Syndrome", "Koberling-Dunnigan Syndrome", "PPARG-related FPLD", "LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3; FPLD3", "Lipodystrophy, Familial Partial, Associated With Pparg Mutations", "LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 3", "Familial partial lipodystrophy type 3", "FPLD3", "Familial partial lipodystrophy"]}
-{"question": "Gene Generalized epidermolysis bullosa simplex has a genetic association with diseases such as", "references": ["KRT14", "CK14", "EBS3", "EBS4", "K14", "NFJ", "keratin 14", "EBS1D", "EBS1", "EBS1B", "EBS1A", "EBS1C", "KRT5", "CK5", "DDD", "DDD1", "EBS2", "K5", "KRT5A", "keratin 5", "EBS2E", "EBS2B", "EBS2C", "EBS1", "EBS2A", "EBS2F", "EBS2D"]}
-{"question": "Gene ZFP57 has a genetic association with diseases such as", "references": ["transient neonatal diabetes mellitus", "Tndm", "Tndm1", "Dmtn", "DIABETES MELLITUS, TRANSIENT NEONATAL, 1", "Diabetes Mellitus, Transient Neonatal, type 1"]}
-{"question": "Gene MANBA has a genetic association with diseases such as", "references": ["beta-mannosidosis", "Beta-D-mannosidosis (disorder)", "beta-mannosidase deficiency", "lysosomal beta-mannosidase deficiency", "Beta-D-mannosidosis", "Beta-Mannosidosis", "MANSB", "MANNOSIDOSIS, BETA A, LYSOSOMAL; MANSB", "MANNOSIDOSIS, BETA A, LYSOSOMAL"]}
-{"question": "Gene RPS6KB1 has a genetic association with diseases such as", "references": ["multiple sclerosis", "MS", "encephalomyelitis disseminata", "insular sclerosis", "disseminated sclerosis", "generalized multiple sclerosis", "Generalized multiple sclerosis (disorder)", "generalised multiple sclerosis", "Multiple sclerosis; MS", "Multiple sclerosis"]}
-{"question": "Gene SERPINI1 has a genetic association with diseases such as", "references": ["familial encephalopathy with neuroserpin inclusion bodies", "FENIB", "ENCEPHALOPATHY, FAMILIAL, WITH NEUROSERPIN INCLUSION BODIES", "Encephalopathy, Familial, With Collins Bodies", "ENCEPHALOPATHY, FAMILIAL, WITH NEUROSERPIN INCLUSION BODIES; FENIB"]}
-{"question": "Gene NT5C1A has a genetic association with diseases such as", "references": ["amyotrophic lateral sclerosis", "ALS", "Lou Gehrig's disease", "motor neuron disease, bulbar", "Lou Gehrig disease", "Charcot disease", "Amyotrophic lateral sclerosis", "motor neurone disease", "Lou Gehrig's disease"]}
-{"question": "Gene SCN9A has a genetic association with diseases such as", "references": ["generalized epilepsy", "Generalised epilepsy", "Epilepsy, Generalized", "idiopathic generalized epilepsy", "Dravet syndrome", "SMEI", "Severe myoclonic epilepsy in infancy", "Severe polymorphic epilepsy of infancy", "Borderland SMEI", "Borderline SMEI", "Intractable childhood epilepsy with generalised tonic clonic seizures", "ICEGTCS", "early infantile epileptic encephalopathy 6", "Dorabe syndrome", "obsolete Dravet syndrome", "dental caries", "dental caries extending into pulp", "dental caries of smooth surface", "dental caries pit and fissure", "tooth decay", "cavities", "caries", "Paroxysmal extreme pain disorder", "Paroxysmal extreme pain disorder\u3001PEPD", "Pain, Submandibular, Ocular, and Rectal, With Flushing", "PEPD", "PAROXYSMAL EXTREME PAIN DISORDER", "Familial rectal pain", "Submandibular, ocular, and rectal pain with flushing", "Rectal Pain, Familial", "Familial rectal syndrome", "Pexpd", "paroxysmal extreme pain disorder"]}
-{"question": "Gene TMEM67 has a genetic association with diseases such as", "references": ["ciliopathy", "ciliopathies"]}
-{"question": "Gene NEIL2 has a genetic association with diseases such as", "references": ["alcohol dependence", "alcoholism", "alcohol dependence syndrome", "alcohol addiction"]}
-{"question": "Gene attention deficit hyperactivity disorder has a genetic association with diseases such as", "references": ["GRIK4", "EAA1", "GRIK", "GluK4", "KA1", "glutamate ionotropic receptor kainate type subunit 4", "GluK4-2", "BCL11A", "BCL11A-L", "BCL11A-S", "BCL11A-XL", "BCL11a-M", "CTIP1", "EVI9", "HBFQTL5", "ZNF856", "B-cell CLL/lymphoma 11A", "DILOS", "B cell CLL/lymphoma 11A", "BCL11A, BAF complex component", "BAF chromatin remodeling complex subunit BCL11A", "SMARCM1", "LRRC7", "DENSIN", "leucine rich repeat containing 7", "SEMA3A", "COLL1", "HH16", "Hsema-I", "Hsema-III", "SEMA1", "SEMAD", "SEMAIII", "SEMAL", "SemD", "coll-1", "semaphorin 3A", "STIP1", "HEL-S-94n", "HOP", "IEF-SSP-3521", "P60", "STI1", "STI1L", "stress induced phosphoprotein 1", "FERMT3", "KIND3", "MIG-2", "MIG2B", "UNC112C", "URP2", "URP2SF", "fermitin family member 3", "FERM domain containing kindlin 3", "EMP2", "NPHS10", "XMP", "epithelial membrane protein 2", "BMPR1B", "ALK-6", "ALK6", "CDw293", "AMDD", "BDA1D", "BDA2", "bone morphogenetic protein receptor type 1B", "AMD3", "FHIT", "AP3Aase", "FRA3B", "fragile histidine triad", "tr\u00edada histidina fr\u00e0gil", "fragile histidine triad diadenosine triphosphatase", "FOXP1", "12CC4", "HSPC215", "MFH", "QRF1", "hFKH1B", "forkhead box P1", "ADAMTS2", "ADAM-TS2", "ADAMTS-2", "ADAMTS-3", "NPI", "PC I-NP", "PCI-NP", "PCINP", "PCPNI", "PNPI", "ADAM metallopeptidase with thrombospondin type 1 motif 2", "EDSDERMS", "SULF2", "HSULF-2", "sulfatase 2", "KIRREL3", "KIRRE", "MRD4", "NEPH2", "PRO4502", "kin of IRRE like 3 (Drosophila)", "Kin of IRRE-like protein 3", "kirre like nephrin family adhesion molecule 3", "PAWR", "Pawr", "2310001G03Rik", "PAR4", "Par-4", "pro-apoptotic WT1 regulator", "ATP8B1", "ATPIC", "BRIC", "FIC1", "ICP1", "PFIC", "PFIC1", "ATPase phospholipid transporting 8B1", "MAP1B", "FUTSCH", "MAP5", "PPP1R102", "microtubule-associated protein 1B", "microtubule associated protein 1B", "PVNH9", "CSMD2", "dJ1007G16.1", "dJ1007G16.2", "dJ947L8.1", "CUB and Sushi multiple domains 2", "DNM1", "Dynamin-1", "DNM", "EIEE31", "dynamin 1", "DEE31", "PPM1F", "CAMKP", "CaMKPase", "FEM-2", "POPX2", "hFEM-2", "protein phosphatase, Mg2+/Mn2+ dependent 1F", "ITGAE", "CD103", "HUMINAE", "integrin subunit alpha E", "MMP24", "MMP-24", "MMP25", "MT-MMP 5", "MT-MMP5", "MT5-MMP", "MT5MMP", "MTMMP5", "matrix metallopeptidase 24", "ITGA11", "HsT18964", "integrin subunit alpha 11", "GPC6", "OMIMD1", "Glypican 6", "MYT1L", "NZF1", "ZC2HC4B", "MRD39", "ZC2H2C2", "myelin transcription factor 1 like", "myT1-L", "REEP5", "C5orf18", "D5S346", "DP1", "TB2", "YOP1", "Yip2e", "receptor accessory protein 5", "POB16", "TLL2", "tolloid like 2", "CREB5", "CRE-BPA", "CREB-5", "cAMP responsive element binding protein 5", "CREBPA", "CDH13", "CDHH", "P105", "cadherin 13", "SUPT3H", "SPT3", "SPT3L", "SPT3 homolog, SAGA and STAGA complex component", "PIWIL4", "HIWI2", "MIWI2", "piwi like RNA-mediated gene silencing 4", "KIF6", "C6orf102", "dJ1043E3.1", "dJ137F1.4", "dJ188D3.1", "kinesin family member 6"]}
-{"question": "Gene ALDH5A1 has a genetic association with diseases such as", "references": ["succinic semialdehyde dehydrogenase deficiency", "4-hydroxybutyric aciduria", "SSADH", "gamma-hydroxybutyric aciduria", "SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY; SSADHD", "Gaba Metabolic Defect", "SSADHD", "Ssadh Deficiency", "Gamma-hydroxybutyricaciduria", "SUCCINIC SEMIALDEHYDE DEHYDROGENASE DEFICIENCY"]}
-{"question": "Gene advanced sleep phase syndrome has a genetic association with diseases such as", "references": ["PER2", "FASPS", "FASPS1", "period circadian clock 2", "period circadian regulator 2"]}
-{"question": "Gene BACH2 has a genetic association with diseases such as", "references": ["type-1 diabetes", "IDDM", "insulin-dependent diabetes mellitus", "type I diabetes mellitus", "T1DM", "insulin dependent diabetes", "juvenile diabetes", "diabetes mellitus juvenile type", "DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM", "Diabetes Mellitus, Type 1", "Diabetes Mellitus, Insulin-Dependent, 1", "DIABETES MELLITUS, INSULIN-DEPENDENT", "Juvenile-Onset Diabetes", "Insulin-Dependent Diabetes Mellitus 1", "diabetes (type 1)", "type 1 diabetes mellitus", "obesity", "corpulence", "overfatness", "fatness", "obese", "vitiligo", "el morenito ojos claros", "multiple sclerosis", "MS", "encephalomyelitis disseminata", "insular sclerosis", "disseminated sclerosis", "generalized multiple sclerosis", "Generalized multiple sclerosis (disorder)", "generalised multiple sclerosis", "Multiple sclerosis; MS", "Multiple sclerosis", "Crohn's disease", "regional enteritis", "Crohn disease", "Crohn's disease of colon (disorder)", "Crohn's disease of large bowel", "Granulomatous Colitis", "regional Ileitis", "regional colitis", "regional enteritis of small intestine with large intestine", "regional enteritis of the large bowel", "regional ileocolitis", "Crohn's disease of colon", "Crohn", "coeliac disease", "celiac sprue", "celiac disease", "nontropical sprue", "endemic sprue", "gluten enteropathy", "idiopathic steatorrhea", "CeD"]}
-{"question": "Gene familial visceral amyloidosis has a genetic association with diseases such as", "references": ["FGA", "Fib2", "fibrinogen alpha chain"]}
-{"question": "Gene Optic nerve hypoplasia has a genetic association with diseases such as", "references": ["PAX6", "AN", "AN2", "D11S812E", "FVH1", "MGDA", "WAGR", "paired box 6", "ASGD5"]}
-{"question": "Gene Neutrophil immunodeficiency syndrome has a genetic association with diseases such as", "references": ["RAC2", "EN-7", "Gx", "HSPC022", "p21-Rac2", "ras-related C3 botulinum toxin substrate 2 (rho family, small GTP binding protein Rac2)", "Rac family small GTPase 2", "IMD73B", "IMD73C", "IMD73A"]}
-{"question": "Gene ETS1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "coeliac disease", "celiac sprue", "celiac disease", "nontropical sprue", "endemic sprue", "gluten enteropathy", "idiopathic steatorrhea", "CeD", "systemic lupus erythematosus", "SLE", "lupus", "Lupus Erythematosus, systemic", "SLE - Lupus Erythematosus, systemic", "disseminated lupus erythematosus", "Systemic lupus erythematosus"]}
-{"question": "Gene STIM2 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene ACO1 has a genetic association with diseases such as", "references": ["asthma", "exercise-induced asthma", "chronic obstructive asthma", "chronic obstructive asthma with status asthmaticus", "chronic obstructive asthma with acute exacerbation", "bronchial hyperreactivity", "Exercise induced asthma", "Asthma", "asthma brionchiole"]}
-{"question": "Gene INAVA has a genetic association with diseases such as", "references": ["ulcerative colitis", "hemorrhagic colitis", "Ulcerative Colitis", "Colitis Ulcerative", "Ulcerative colitis", "left-sided ulcerative colitis", "UC"]}
-{"question": "Gene EYA1 has a genetic association with diseases such as", "references": ["chronic obstructive pulmonary disease", "COPD", "chronic obstructive airway disease", "chronic obstructive airways disease NOS", "chronic obstructive lung disease", "chronic obstructive airways disease NOS disorder", "chronic obstructive lung disease disorder", "COLD", "COLD (chronic obstructive lung disease)", "Chronic Obstructive Pulmonary Disease, (COPD)", "Pulmonary Disease (COPD), Chronic Obstructive", "Obstructive Pulmonary Disease (COPD), Chronic", "Chronic Obstructive Airways Disease", "Disease (COPD), Chronic Obstructive", "Chronic Obstructive Pulmonary Disease (COPD)", "obstructive lung disease, chronic", "COPD, Chronic Obstructive Pulmonary Disease", "Pulmonary Disease, Chronic Obstructive", "branchiootorenal syndrome", "Branchio-Oto-renal syndrome", "Branchio-otorenal dysplasia", "Melnick-Fraser syndrome (disorder)", "branchiootorenal dysplasia", "Melnick-Fraser syndrome", "BOR syndrome", "Branchiootorenal syndrome"]}
-{"question": "Gene ICA1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene benign familial infantile epilepsy has a genetic association with diseases such as", "references": ["PRRT2", "BFIC2", "BFIS2", "DSPB3", "DYT10", "EKD1", "FICCA", "ICCA", "IFITMD1", "PKC", "proline rich transmembrane protein 2", "SCN2A", "BFIC3", "BFIS3", "BFNIS", "EIEE11", "HBA", "HBSCI", "HBSCII", "NAC2", "Na(v)1.2", "Nav1.2", "SCN2A1", "SCN2A2", "sodium voltage-gated channel alpha subunit 2", "DEE11", "EA9"]}
-{"question": "Gene TERT has a genetic association with diseases such as", "references": ["breast cancer", "malignant neoplasm of breast", "malignant tumor of the breast", "mammary cancer", "primary breast cancer", "breast disorder", "interstitial lung disease", "ILD", "interstitial pneumonitis", "Lung Diseases, Interstitial", "adenocarcinoma of the lung", "lung adenocarcinoma", "nonsmall cell adenocarcinoma", "adenocarcinoma of lung", "bronchogenic lung adenocarcinoma", "Adenocarcinoma of the Lung", "non-small cell lung adenocarcinoma", "pulmonary adenocarcinoma", "prostate cancer", "malignant tumor of the prostate", "prostatic cancer", "tumor of the prostate", "malignant neoplasm of the prostate", "prostate cancer, familial", "hereditary prostate cancer", "lung cancer", "malignant lung tumor", "malignant neoplasm of lung", "idiopathic pulmonary fibrosis", "FIBROCYSTIC PULMONARY DYSPLASIA", "IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL", "cryptogenic fibrosing alveolitis"]}
-{"question": "Gene GAA has a genetic association with diseases such as", "references": ["glycogen storage disease II", "Pompe disease", "acid maltase deficiency", "Generalized glycogenosis (disorder)", "Glycogen storage disease, type II (disorder)", "Glycogenosis, type 2", "Lysosomal alpha-1,4-glucosidase deficiency (disorder)", "Pompe's disease", "deficiency of glucoamylase", "deficiency of maltase", "glycogen storage disease type II", "Lysosomal alpha-1,4-glucosidase deficiency", "Glycogen storage disease, type II", "Generalized glycogenosis", "Glycogen storage disease type 2", "Alpha-1,4-glucosidase acid deficiency", "GLYCOGEN STORAGE DISEASE II", "Gsd 2", "Glycogenosis type 2", "Gaa Deficiency", "Cardiomegalia Glycogenica Diffusa", "GSD2", "GSD type II", "GSD due to acid maltase deficiency", "GSD type 2", "Glycogenosis type II", "Glycogenosis due to acid maltase deficiency", "Alpha-1,4-Glucosidase Deficiency", "GLYCOGEN STORAGE DISEASE II; GSD2", "Glycogen storage disease due to acid maltase deficiency", "Glycogenosis, Generalized, Cardiac Form"]}
-{"question": "Gene gastrointestinal stromal tumor has a genetic association with diseases such as", "references": ["PDGFRA", "CD140A", "PDGFR-2", "PDGFR2", "RHEPDGFRA", "GAS9", "platelet derived growth factor receptor alpha"]}
-{"question": "Gene Rothmund-Thomson syndrome has a genetic association with diseases such as", "references": ["RECQL4", "RECQ4", "RecQ like helicase 4"]}
-{"question": "Gene Kowarski syndrome has a genetic association with diseases such as", "references": ["GH1", "GH", "GH-N", "GHN", "IGHD1B", "hGH-N", "GHB5", "Growth hormone 1", "IGHD2", "IGHD1A"]}
-{"question": "Gene Menkes disease has a genetic association with diseases such as", "references": ["ATP7A", "DSMAX", "MK", "MNK", "SMAX3", "ATPase copper transporting alpha"]}
-{"question": "Gene MonoMAC has a genetic association with diseases such as", "references": ["GATA2", "DCML", "IMD21", "MONOMAC", "NFE1B", "GATA binding protein 2"]}
-{"question": "Gene DPYSL5 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene IL6R has a genetic association with diseases such as", "references": ["rheumatoid arthritis", "Arthritis or polyarthritis, rheumatic", "atrophic Arthritis", "Rheumatoid arthritis with vasculitis", "Malignant rheumatoid arthritis", "Rheumatoid arthritis", "asthma", "exercise-induced asthma", "chronic obstructive asthma", "chronic obstructive asthma with status asthmaticus", "chronic obstructive asthma with acute exacerbation", "bronchial hyperreactivity", "Exercise induced asthma", "Asthma", "asthma brionchiole"]}
-{"question": "Gene ZFYVE26 has a genetic association with diseases such as", "references": ["amyotrophic lateral sclerosis", "ALS", "Lou Gehrig's disease", "motor neuron disease, bulbar", "Lou Gehrig disease", "Charcot disease", "Amyotrophic lateral sclerosis", "motor neurone disease", "Lou Gehrig's disease"]}
-{"question": "Gene DiGeorge syndrome has a genetic association with diseases such as", "references": ["TBX1", "CAFS", "CATCH22", "CTHM", "DGCR", "DGS", "DORV", "TBX1C", "TGA", "VCF", "VCFS", "T-box 1", "T-box transcription factor 1"]}
-{"question": "Gene Clouston syndrome has a genetic association with diseases such as", "references": ["GJB6", "CX30", "DFNA3", "DFNA3B", "DFNB1B", "ECTD2", "ED2", "EDH", "HED", "HED2", "gap junction protein beta 6"]}
-{"question": "Gene MTF1 has a genetic association with diseases such as", "references": ["hypothyroidism", "Thyroid insufficiency", "underactive thyroid", "low thyroid", "hypothyreosis", "Thyroid \u0410\u043d\u0430\u0441\u0442\u0430\u0441\u0438\u044f deficiency"]}
-{"question": "Gene erythromelalgia has a genetic association with diseases such as", "references": ["SCN9A", "ETHA", "FEB3B", "GEFSP7", "HSAN2D", "NE-NA", "NENA", "Nav1.7", "PN1", "SFNP", "sodium voltage-gated channel alpha subunit 9"]}
-{"question": "Gene CBX7 has a genetic association with diseases such as", "references": ["multiple myeloma", "plasma cell myeloma"]}
-{"question": "Gene ANXA5 has a genetic association with diseases such as", "references": ["chronic obstructive pulmonary disease", "COPD", "chronic obstructive airway disease", "chronic obstructive airways disease NOS", "chronic obstructive lung disease", "chronic obstructive airways disease NOS disorder", "chronic obstructive lung disease disorder", "COLD", "COLD (chronic obstructive lung disease)", "Chronic Obstructive Pulmonary Disease, (COPD)", "Pulmonary Disease (COPD), Chronic Obstructive", "Obstructive Pulmonary Disease (COPD), Chronic", "Chronic Obstructive Airways Disease", "Disease (COPD), Chronic Obstructive", "Chronic Obstructive Pulmonary Disease (COPD)", "obstructive lung disease, chronic", "COPD, Chronic Obstructive Pulmonary Disease", "Pulmonary Disease, Chronic Obstructive"]}
-{"question": "Gene MMP24 has a genetic association with diseases such as", "references": ["attention deficit hyperactivity disorder", "ADHD", "hyperkinetic disorder", "attention deficit disorder", "AD/HD", "A.D.H.D", "attention deficit/hyperactivity disorder", "attention deficit hyperactivity syndrome", "Attention Deficit Disorder with Hyperactivity", "ADDH"]}
-{"question": "Gene arterial tortuosity syndrome has a genetic association with diseases such as", "references": ["SLC2A10", "ATS", "GLUT10", "solute carrier family 2 member 10", "ATORS"]}
-{"question": "Gene ARHGEF3 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "rheumatoid arthritis", "Arthritis or polyarthritis, rheumatic", "atrophic Arthritis", "Rheumatoid arthritis with vasculitis", "Malignant rheumatoid arthritis", "Rheumatoid arthritis"]}
-{"question": "Gene PARP8 has a genetic association with diseases such as", "references": ["myopia", "near-sightedness", "short-sightedness", "near vision"]}
-{"question": "Gene Timothy syndrome has a genetic association with diseases such as", "references": ["CACNA1C", "CACH2", "CACN2", "CACNL1A1", "CCHL1A1", "CaV1.2", "LQT8", "TS", "calcium voltage-gated channel subunit alpha1 C", "TS. LQT8"]}
-{"question": "Gene POLE has a genetic association with diseases such as", "references": ["Polymerase proofreading-related adenomatous polyposis", "PPAP", "Polymerase proofreading-associated polyposis"]}
-{"question": "Gene acute lymphocytic leukemia has a genetic association with diseases such as", "references": ["PIP4K2A", "PI5P4KA", "PIP5K2A", "PIP5KII-alpha", "PIP5KIIA", "PIPK", "phosphatidylinositol-5-phosphate 4-kinase type 2 alpha", "GATA3", "HDR", "HDRS", "GATA binding protein 3", "ARID5B", "DESRT", "MRF-2", "MRF2", "AT-rich interaction domain 5B", "CEBPE", "C/EBP-epsilon", "CRP1", "CCAAT/enhancer binding protein epsilon", "CCAAT enhancer binding protein epsilon", "c/EBP epsilon", "IKZF1", "Hs.54452", "IK1", "IKAROS", "LYF1", "LyF-1", "PPP1R92", "PRO0758", "ZNFN1A1", "CVID13", "IKAROS family zinc finger 1"]}
-{"question": "Gene ATP1A2 has a genetic association with diseases such as", "references": ["alternating hemiplegia of childhood", "AHC", "Alternating Hemiplegia of Childhood type 1", "ALTERNATING HEMIPLEGIA OF CHILDHOOD 1; AHC1", "ALTERNATING HEMIPLEGIA OF CHILDHOOD 1", "AHC1"]}
-{"question": "Gene progressive nonfluent aphasia has a genetic association with diseases such as", "references": ["GRN", "CLN11", "GEP", "GP88", "PCDGF", "PEPI", "PGRN", "Granulin", "granulin precursor"]}
-{"question": "Gene hypoparathyroidism-retardation-dysmorphism syndrome has a genetic association with diseases such as", "references": ["TBCE", "HRD", "KCS", "KCS1", "pac2", "tubulin folding cofactor E", "PEAMO"]}
-{"question": "Gene MYO5B has a genetic association with diseases such as", "references": ["microvillus inclusion disease", "Davidson disease", "MVD", "congenital familial protracted diarrhea with enterocyte brush-border abnormalities", "congenital microvillus atrophy", "diarrhea 2 with microvillus atrophy", "intractable diarrhea of infancy", "Microvillous inclusion disease", "DIARRHEA 2, WITH MICROVILLUS ATROPHY; DIAR2", "Microvillus Inclusion Disease", "MVID", "Microvillus Atrophy, Congenital", "Congenital microvillous atrophy", "DIARRHEA 2, WITH MICROVILLUS ATROPHY", "DIAR2"]}
-{"question": "Gene dihydropyrimidine dehydrogenase deficiency has a genetic association with diseases such as", "references": ["DPYD", "DHP", "DHPDHASE", "DPD", "dihydropyrimidine dehydrogenase", "DYPD"]}
-{"question": "Gene congenital hereditary endothelial dystrophy of cornea has a genetic association with diseases such as", "references": ["SLC4A11", "BTR1", "CDPD1", "CHED2", "NABC1", "dJ794I6.2", "CHED", "solute carrier family 4 member 11"]}
-{"question": "Gene TAFA5 has a genetic association with diseases such as", "references": ["pancreatic cancer", "Ca tail of pancreas", "Ca head of pancreas", "Ca body of pancreas", "malignant neoplasm of head of pancreas", "malignant neoplasm of tail of pancreas", "malignant neoplasm of body of pancreas"]}
-{"question": "Gene Shwachman-Diamond syndrome has a genetic association with diseases such as", "references": ["SBDS", "SDS", "SWDS", "CGI-97", "SBDS ribosome assembly guanine nucleotide exchange factor", "SBDS, ribosome maturation factor", "SBDS ribosome maturation factor", "SDO1"]}
-{"question": "Gene SBF2 has a genetic association with diseases such as", "references": ["pancreatic cancer", "Ca tail of pancreas", "Ca head of pancreas", "Ca body of pancreas", "malignant neoplasm of head of pancreas", "malignant neoplasm of tail of pancreas", "malignant neoplasm of body of pancreas"]}
-{"question": "Gene MPZL1 has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene COX1 has a genetic association with diseases such as", "references": ["Leber hereditary optic neuropathy", "LHON", "Leber optic atrophy", "Leber's optic atrophy", "Leber's optic atrophy (disorder)", "optic atrophy, Leber's", "Leber's hereditary optic neuropathy", "Laber'shereditary optic neuropathy", "Leber Hereditary Optic Neuropathy", "Optic Atrophy, Hereditary, Leber", "colorectal cancer", "colon cancer", "rectal cancer", "large intestine cancer", "Colorectal cancer, familial", "bowel cancer", "colon and rectal cancer"]}
-{"question": "Gene DOCK3 has a genetic association with diseases such as", "references": ["melanoma", "malignant melanoma", "Naevocarcinom", "Naevocarcinoma", "MELANOMA, MALIGNANT", "Melanoma"]}
-{"question": "Gene IL36RN has a genetic association with diseases such as", "references": ["Generalized pustular psoriasis", "psoriasis 14, pustular", "Acrodermatitis Continua of Hallopeau", "Generalized Pustular Psoriasis", "Psorp", "PSORS14", "PSORIASIS 14, PUSTULAR; PSORS14", "PSORIASIS 14, PUSTULAR", "Interleukin 36 Receptor Antagonist Deficiency", "Palmoplantar Pustulosis", "generalized pustular psoriasis", "GPP"]}
-{"question": "Gene AP1S1 has a genetic association with diseases such as", "references": ["MEDNIK syndrome", "erythrokeratodermia variabilis 3", "erythrokeratodermia variabilis, Kamouraska type", "mental retardation, enteropathy, deafness, neuropathy, ichthyosis, keratodermia", "MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA; MEDNIK", "MENTAL RETARDATION, ENTEROPATHY, DEAFNESS, PERIPHERAL NEUROPATHY, ICHTHYOSIS, AND KERATODERMA", "Intellectual disability-enteropathy-deafness-peripheral neuropathy-ichthyosis-keratodermia syndrome", "MEDNIK", "MEDNIK Syndrome"]}
-{"question": "Gene CNTNAP2 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease", "bipolar disorder", "BP", "manic depression", "BPAD", "schizophrenia", "Morel-Kraepelin disease", "Kraepelin-Morel disease", "dementia pr\u00e6cox", "dementia praecox", "schizophrenia-1"]}
-{"question": "Gene Wolff-Parkinson-White syndrome has a genetic association with diseases such as", "references": ["PRKAG2", "AAKG", "AAKG2", "CMH6", "H91620p", "WPWS", "protein kinase AMP-activated non-catalytic subunit gamma 2"]}
-{"question": "Gene EDNRA has a genetic association with diseases such as", "references": ["intracranial aneurysm", "brain aneurysm", "Intracranial aneurysm", "cerebral aneurysm"]}
-{"question": "Gene GRACILE syndrome has a genetic association with diseases such as", "references": ["BCS1L", "BCS", "BCS1", "BJS", "FLNMS", "GRACILE", "Hs.6719", "MC3DN1", "PTD", "h-BCS", "h-BCS1", "BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone"]}
-{"question": "Gene M\u00fcllerian agenesis has a genetic association with diseases such as", "references": ["WNT4", "SERKAL", "WNT-4", "Wnt family member 4"]}
-{"question": "Gene MBTPS2 has a genetic association with diseases such as", "references": ["Ichthyosis follicularis with alopecia and photophobia syndrome", "IFAP syndrome", "IFAP SYNDROME WITH OR WITHOUT BRESHECK SYNDROME", "Ichthyosis follicularis-atrichia-photophobia syndrome", "Ichthyosis Follicularis, Atrichia, and Photophobia With or Without Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear/Eye Anomalies, Cleft Palate/Cryptorchidism, and Kidney Dysplasia/Hypoplasia", "IFAP syndromea"]}
-{"question": "Gene PPP4R3B has a genetic association with diseases such as", "references": ["metabolic disease", "metabolic illness", "disorder of metabolic process", "metabolic disorder", "metabolic diseases", "disease of metabolism"]}
-{"question": "Gene 17-beta-hydroxysteroid dehydrogenase deficiency has a genetic association with diseases such as", "references": ["HSD17B3", "EDH17B3", "SDR12C2", "hydroxysteroid (17-beta) dehydrogenase 3", "hydroxysteroid 17-beta dehydrogenase 3"]}
-{"question": "Gene MSI2 has a genetic association with diseases such as", "references": ["coronary artery disease", "CAD", "atherosclerotic heart disease", "coronary heart disease", "ischemic heart disease", "IHD", "atherosclerotic cardiovascular disease", "CHD (coronary heart disease)", "coronary arteriosclerosis", "CHD", "coronary artery arteriosclerosis (disease)", "atherosclerosis of coronary artery", "Coronary Atherosclerosis"]}
-{"question": "Gene RAB14 has a genetic association with diseases such as", "references": ["smallpox", "ordinary smallpox", "variola", "variola vera"]}
-{"question": "Gene eosinophilic esophagitis has a genetic association with diseases such as", "references": ["STAT6", "D12S1644", "IL-4-STAT", "STAT6B", "STAT6C", "signal transducer and activator of transcription 6", "DSG1", "CDHF4", "DG1", "DSG", "EPKHE", "EPKHIA", "PPKS1", "SPPK1", "desmoglein 1"]}
-{"question": "Gene CD2AP has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene progeroid features-hepatocellular carcinoma predisposition syndrome has a genetic association with diseases such as", "references": ["SPRTN", "C1orf124", "DDDL1880", "DVC1", "PRO4323", "Spartan", "dJ876B10.3", "SprT-like N-terminal domain"]}
-{"question": "Gene ADAM12 has a genetic association with diseases such as", "references": ["endometrial cancer", "endometrial Ca", "malignant endometrial neoplasm", "malignant neoplasm of endometrium", "neoplasm of endometrium (disorder)", "primary malignant neoplasm of endometrium", "tumor of Endometrium", "Endometrial Tumor", "endometrium tumor", "endometrium neoplasm (disease)", "Tumor of the Endometrium"]}
-{"question": "Gene SIX1 has a genetic association with diseases such as", "references": ["branchiootorenal syndrome", "Branchio-Oto-renal syndrome", "Branchio-otorenal dysplasia", "Melnick-Fraser syndrome (disorder)", "branchiootorenal dysplasia", "Melnick-Fraser syndrome", "BOR syndrome", "Branchiootorenal syndrome"]}
-{"question": "Gene double outlet right ventricle has a genetic association with diseases such as", "references": ["GATA6", "GATA binding protein 6", "NKX2-5", "CHNG5", "CSX", "CSX1", "HLHS2", "NKX2.5", "NKX2E", "NKX4-1", "VSD3", "NK2 homeobox 5"]}
-{"question": "Gene limb-girdle muscular dystrophy has a genetic association with diseases such as", "references": ["CAPN3", "CANP3", "CANPL3", "LGMD2", "LGMD2A", "nCL-1", "p94", "calpain 3", "LGMDR1", "LGMDD4"]}
-{"question": "Gene KMO has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene C8orf34 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "non-small-cell lung carcinoma", "NSCLC", "non-small cell lung carcinoma", "Non-small cell lung cancer (disorder)", "Non-small cell lung cancer", "Non Small Cell Lung Cancer NOS", "Non-small cell lung cancer, NOS", "Non-Small Cell Cancer of the Lung", "NSCLC - Non-Small Cell Lung Cancer", "Non-Small Cell Carcinoma of Lung", "Non-Small Cell Carcinoma of the Lung", "Non-Small Cell Cancer of Lung", "Carcinoma, Non-Small-Cell Lung", "lung non-small cell carcinoma", "non-small cell lung cancer"]}
-{"question": "Gene ATP8B1 has a genetic association with diseases such as", "references": ["vitiligo", "el morenito ojos claros", "attention deficit hyperactivity disorder", "ADHD", "hyperkinetic disorder", "attention deficit disorder", "AD/HD", "A.D.H.D", "attention deficit/hyperactivity disorder", "attention deficit hyperactivity syndrome", "Attention Deficit Disorder with Hyperactivity", "ADDH", "conduct disorder", "disruptive behavior disorder"]}
-{"question": "Gene PBRM1 has a genetic association with diseases such as", "references": ["mood disorders", "episodic mood disorder", "affective psychosis", "affective disorder", "mood [affective] disorders", "mood disorder"]}
-{"question": "Gene hemolytic anemia has a genetic association with diseases such as", "references": ["NT5C3A", "NT5C3", "P5'N-1", "P5N-1", "PN-I", "POMP", "PSN1", "UMPH", "UMPH1", "cN-III", "hUMP1", "p36", "5'-nucleotidase, cytosolic IIIA"]}
-{"question": "Gene hepatitis B has a genetic association with diseases such as", "references": ["HLA-DQB2", "HLA-DQB1", "HLA-DXB", "major histocompatibility complex, class II, DQ beta 2", "DQB2", "UBE2L3", "E2-F1", "L-UBC", "UBCH7", "UbcM4", "ubiquitin conjugating enzyme E2 L3", "HLA-DPB1", "DPB1", "HLA-DP", "HLA-DP1B", "HLA-DPB", "major histocompatibility complex, class II, DP beta 1", "GRIN2A", "EPND", "FESD", "GluN2A", "LKS", "NMDAR2A", "NR2A", "glutamate ionotropic receptor NMDA type subunit 2A"]}
-{"question": "Gene RXRG has a genetic association with diseases such as", "references": ["HIV/AIDS", "acquired Immune deficiency", "acquired immune deficiency syndrome", "AIDS, Acquired Immunodeficiency Syndrome", "Acquired Immunodeficiency Disease", "Acquired Immunodeficiency Syndrome, AIDS", "acquired immunodeficiency syndrome", "AIDS"]}
-{"question": "Gene DNAH5 has a genetic association with diseases such as", "references": ["astigmatism", "allergy", "hypersensitivity", "allergies", "allergic disease", "Immunologic diseases. Allergy", "GO:0016068", "atherosclerosis", "arteriosclerotic vascular disease", "ASVD"]}
-{"question": "Gene failure of eruption of teeth has a genetic association with diseases such as", "references": ["PTH1R", "PFE", "PTHR", "PTHR1", "Parathyroid hormone 1 receptor", "EKNS"]}
-{"question": "Gene central core myopathy has a genetic association with diseases such as", "references": ["RYR1", "CCO", "MHS", "MHS1", "PPP1R137", "RYDR", "RYR", "RYR-1", "SKRR", "ryanodine receptor 1", "KDS"]}
-{"question": "Gene Megalencephalic leukoencephalopathy with subcortical cysts has a genetic association with diseases such as", "references": ["MLC1", "LVM", "MLC", "VL", "megalencephalic leukoencephalopathy with subcortical cysts 1", "modulator of VRAC current 1"]}
-{"question": "Gene Pick disease has a genetic association with diseases such as", "references": ["PSEN1", "Psen1", "Ad3h", "PS-1", "PS1", "S182", "AD3", "FAD", "presenilin 1", "ACNINV3"]}
-{"question": "Gene Adams-Oliver syndrome has a genetic association with diseases such as", "references": ["RBPJ", "AOS3", "CBF1", "IGKJRB", "IGKJRB1", "KBF2", "RBP-J", "RBPJK", "RBPSUH", "SUH", "csl", "recombination signal binding protein for immunoglobulin kappa J region", "RBP-J kappa", "RBP-JK", "CBF-1", "DLL4", "hdelta2", "AOS6", "delta like canonical Notch ligand 4", "delta4", "NOTCH1", "Notch1", "9930111A19Rik", "Mis6", "N1", "Tan1", "lin-12", "AOS5", "AOVD1", "hN1", "notch 1", "notch receptor 1", "DOCK6", "AOS2", "ZIR1", "Dock6", "dedicator of cytokinesis 6", "ARHGAP31", "AOS1", "CDGAP", "Rho GTPase activating protein 31"]}
-{"question": "Gene ALDH3A2 has a genetic association with diseases such as", "references": ["Sjogren-Larsson syndrome", "Sjogren Larsson syndrome", "Sjogren-Larsson syndrome (disorder)", "Sjogren-Larsson's syndrome", "Sj\u00f6gren-Larsson syndrome", "Fatty Alcohol:Nad+ Oxidoreductase Deficiency", "FAO deficiency", "Faldh Deficiency", "SJOGREN-LARSSON SYNDROME; SLS", "FADH deficiency", "Fatty acid alcohol oxidoreductase deficiency", "SLS", "SJOGREN-LARSSON SYNDROME", "Ichthyosis, Spastic Neurologic Disorder, and Oligophrenia", "Fatty Aldehyde Dehydrogenase Deficiency"]}
-{"question": "Gene Fazio-Londe disease has a genetic association with diseases such as", "references": ["SLC52A3", "BVVLS", "BVVLS1", "C20orf54", "RFT2", "RFVT3", "bA371L19.1", "hRFT2", "solute carrier family 52 member 3"]}
-{"question": "Gene CEP72 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene beta-ketothiolase deficiency has a genetic association with diseases such as", "references": ["ACAT1", "ACAT", "MAT", "T2", "THIL", "acetyl-CoA acetyltransferase 1"]}
-{"question": "Gene familial atrial fibrillation has a genetic association with diseases such as", "references": ["KCNQ1", "ATFB1", "ATFB3", "JLNS1", "KCNA8", "KCNA9", "KVLQT1", "Kv1.9", "Kv7.1", "LQT", "LQT1", "RWS", "SQT2", "WRS", "potassium voltage-gated channel subfamily Q member 1", "SCN5A", "CDCD2", "CMD1E", "CMPD2", "HB1", "HB2", "HBBD", "HH1", "ICCD", "IVF", "LQT3", "Nav1.5", "PFHB1", "SSS1", "VF1", "sodium voltage-gated channel alpha subunit 5", "KCNJ2", "ATFB9", "HHBIRK1", "HHIRK1", "IRK1", "KIR2.1", "LQT7", "SQT3", "potassium voltage-gated channel subfamily J member 2", "potassium inwardly rectifying channel subfamily J member 2", "ABCC9", "ABC37", "ATFB12", "CANTU", "CMD1O", "SUR2", "ATP binding cassette subfamily C member 9", "NPPA", "ANF", "ANP", "ATFB6", "ATRST2", "CDD", "CDD-ANF", "CDP", "PND", "Atrial natriuretic peptide", "natriuretic peptide A", "KCNA5", "ATFB7", "HCK1", "HK2", "HPCN1", "KV1.5", "PCN1", "potassium voltage-gated channel subfamily A member 5", "KCNE2", "ATFB4", "LQT5", "LQT6", "MIRP1", "potassium voltage-gated channel subfamily E regulatory subunit 2", "SCN2B", "ATFB14", "sodium voltage-gated channel beta subunit 2", "SCN1B", "ATFB13", "BRGDA5", "GEFSP1", "sodium voltage-gated channel beta subunit 1", "EIEE52", "DEE52", "GJA5", "ATFB11", "CX40", "gap junction protein alpha 5"]}
-{"question": "Gene Morning glory disc anomaly has a genetic association with diseases such as", "references": ["PAX6", "AN", "AN2", "D11S812E", "FVH1", "MGDA", "WAGR", "paired box 6", "ASGD5"]}
-{"question": "Gene Gillespie syndrome has a genetic association with diseases such as", "references": ["ITPR1", "ACV", "CLA4", "INSP3R1", "IP3R", "IP3R1", "PPP1R94", "SCA15", "SCA16", "SCA29", "inositol 1,4,5-trisphosphate receptor type 1"]}
-{"question": "Gene periodontitis has a genetic association with diseases such as", "references": ["TIMP2", "CSC-21K", "DDC8", "TIMP metallopeptidase inhibitor 2", "ACTN2", "CMD1AA", "CMH23", "actinin alpha 2", "MYOCOZ", "MPD6", "IGF2R", "CD222", "CIMPR", "M6P-R", "MPR1", "MPRI", "M6P/IGF2R", "MPR 300", "CI-M6PR", "MPR300", "insulin like growth factor 2 receptor", "CSMD1", "PPP1R24", "CUB and Sushi multiple domains 1", "LRP1B", "LRP-DIT", "LRPDIT", "LDL receptor related protein 1B", "LRP-1B", "KDM4B", "JMJD2B", "TDRD14B", "lysine demethylase 4B", "MRD65", "HLA-DOA", "HLA-DNA", "HLA-DZA", "HLADZ", "major histocompatibility complex, class II, DO alpha", "ITGA8", "integrin subunit alpha 8", "NLGN1", "NL1", "neuroligin 1", "LBP", "BPIFD2", "lipopolysaccharide binding protein", "KCNJ16", "BIR9", "KIR5.1", "potassium voltage-gated channel subfamily J member 16", "potassium inwardly rectifying channel subfamily J member 16", "HKTD", "SCN2A", "BFIC3", "BFIS3", "BFNIS", "EIEE11", "HBA", "HBSCI", "HBSCII", "NAC2", "Na(v)1.2", "Nav1.2", "SCN2A1", "SCN2A2", "sodium voltage-gated channel alpha subunit 2", "DEE11", "EA9", "TGIF1", "HPE4", "TGIF", "TGFB induced factor homeobox 1", "GRIK1", "EAA3", "EEA3", "GLR5", "GLUR5", "GluK1", "gluR-5", "glutamate ionotropic receptor kainate type subunit 1", "CDH13", "CDHH", "P105", "cadherin 13", "HS6ST2", "heparan sulfate 6-O-sulfotransferase 2", "MRXSPM", "PTPRT", "RPTPrho", "protein tyrosine phosphatase, receptor type T", "protein tyrosine phosphatase receptor type T", "RPTP-rho", "R-PTP-T", "PSMA8", "PSMA7L", "proteasome subunit alpha 8", "proteasome 20S subunit alpha 8", "ERC2", "CAST", "CAST1", "ELKSL", "SPBC110", "Spc110", "ELKS/RAB6-interacting/CAST family member 2", "ACTN1", "BDPLT15", "actinin alpha 1", "FAM135B", "C8ORFK32", "family with sequence similarity 135 member B", "ROBO2", "SAX3", "roundabout guidance receptor 2", "CTSC", "CPPI", "DPP-I", "DPP1", "DPPI", "HMS", "JP", "JPD", "PALS", "PDON1", "PLS", "cathepsin C"]}
-{"question": "Gene XPR1 has a genetic association with diseases such as", "references": ["asthma", "exercise-induced asthma", "chronic obstructive asthma", "chronic obstructive asthma with status asthmaticus", "chronic obstructive asthma with acute exacerbation", "bronchial hyperreactivity", "Exercise induced asthma", "Asthma", "asthma brionchiole"]}
-{"question": "Gene sitosterolemia has a genetic association with diseases such as", "references": ["ABCG8", "GBD4", "STSL", "ATP binding cassette subfamily G member 8", "STSL1", "ABCG5", "STSL", "ATP binding cassette subfamily G member 5", "STSL2"]}
-{"question": "Gene NKX2-5 has a genetic association with diseases such as", "references": ["tetralogy of Fallot", "Ventricular septal defect with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle", "TOF", "Fallot tetralogy", "TETRALOGY OF FALLOT", "TETRALOGY OF FALLOT; TOF"]}
-{"question": "Gene lysinuric protein intolerance has a genetic association with diseases such as", "references": ["SLC7A7", "LAT3", "LPI", "MOP-2", "Y+LAT1", "y+LAT-1", "solute carrier family 7 member 7"]}
-{"question": "Gene KRAS has a genetic association with diseases such as", "references": ["acute myeloid leukemia", "AML - acute Myeloid Leukemia", "Leukemia, Myelocytic, acute", "acute myeloblastic leukemia", "acute myelogenous leukemia", "Acute myelogenous leukemia; AML", "Acute Granulocytic Leukemia", "LEUKEMIA, ACUTE MYELOID; AML", "Acute non lymphoblastic leukemia", "myeloid leukemia, acute", "LEUKEMIA, ACUTE MYELOID", "ANLL", "Hematopoeitic - Acute Myleogenous Leukemia (AML)", "Acute Myeloid Leukemia", "Leukemia, Acute Myeloid, Susceptibility to", "Acute Myeloid Leukemia (AML)", "Leukemia, Acute Myelogenous", "Acute Myelogenous Leukemias", "AML", "Acute Nonlymphocytic Leukemia", "Acute Myelocytic Leukemia", "acute myeloid leukaemia", "juvenile myelomonocytic leukemia", "Juvenile Chronic Myeloid Leukemia", "Juvenile Myelomonocytic Leukemia", "Juvenile chronic myelomonocytic leukemia", "Chronic Myelomonocytic Leukemia", "JUVENILE MYELOMONOCYTIC LEUKEMIA; JMML", "Juvenile Chronic Myelogenous Leukemia", "JCML", "Leukemia, Chronic Myelomonocytic", "Leukemia, Juvenile Myelomonocytic", "JMML"]}
-{"question": "Gene UBASH3A has a genetic association with diseases such as", "references": ["rheumatoid arthritis", "Arthritis or polyarthritis, rheumatic", "atrophic Arthritis", "Rheumatoid arthritis with vasculitis", "Malignant rheumatoid arthritis", "Rheumatoid arthritis", "type-1 diabetes", "IDDM", "insulin-dependent diabetes mellitus", "type I diabetes mellitus", "T1DM", "insulin dependent diabetes", "juvenile diabetes", "diabetes mellitus juvenile type", "DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM", "Diabetes Mellitus, Type 1", "Diabetes Mellitus, Insulin-Dependent, 1", "DIABETES MELLITUS, INSULIN-DEPENDENT", "Juvenile-Onset Diabetes", "Insulin-Dependent Diabetes Mellitus 1", "diabetes (type 1)", "type 1 diabetes mellitus", "coeliac disease", "celiac sprue", "celiac disease", "nontropical sprue", "endemic sprue", "gluten enteropathy", "idiopathic steatorrhea", "CeD", "vitiligo", "el morenito ojos claros"]}
-{"question": "Gene Cenani-Lenz syndactyly syndrome has a genetic association with diseases such as", "references": ["LRP4", "CLSS", "LRP-4", "LRP10", "MEGF7", "SOST2", "CMS17", "Low density lipoprotein receptor-related protein 4", "LDL receptor related protein 4"]}
-{"question": "Gene WRN has a genetic association with diseases such as", "references": ["Werner syndrome", "WS", "Werner's syndrome", "adult premature ageing syndrome", "adult progeria", "WERNER SYNDROME; WRN", "WRN", "WERNER SYNDROME", "colorectal cancer", "colon cancer", "rectal cancer", "large intestine cancer", "Colorectal cancer, familial", "bowel cancer", "colon and rectal cancer"]}
-{"question": "Gene GIPR has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene microphthalmia has a genetic association with diseases such as", "references": ["HCCS", "CCHL", "MCOPS7", "MLS", "LSDMCA1", "holocytochrome c synthase", "BMP4", "BMP2B", "BMP2B1", "MCOPS6", "OFC11", "ZYME", "bone morphogenetic protein 4", "TMEM98", "NNO4", "TADA1", "transmembrane protein 98", "OTX2", "CPHD6", "MCOPS5", "Orthodenticle homeobox 2", "MFRP", "MCOP5", "NNO2", "RD6", "membrane frizzled-related protein", "CTRP5"]}
-{"question": "Gene ATRX has a genetic association with diseases such as", "references": ["Alpha-thalassemia mental retardation syndrome", "ATR-X syndrome", "alpha thalassemia-X-linked intellectual disability syndrome", "ATR, nondeletion type", "alpha-thalassemia/mental retardation syndrome nondeletion type", "ATRX syndrome", "Alpha-thalassemia x-linked intellectual disability syndrome", "ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED", "Alpha-thalassemia-X-linked intellectual disability syndrome", "Alpha Thalassemia/Mental Retardation Syndrome X-Linked", "Alpha Thalassemia X-Linked Mental Retardation Syndrome", "Alpha-Thalassemia/Mental Retardation Syndrome, Nondeletion Type", "Alpha thalassemia mental retardation syndrome, nondeletion type, X-linked", "XLMR hypotonic face syndrome", "ATRX", "ALPHA-THALASSEMIA/MENTAL RETARDATION SYNDROME, X-LINKED; ATRX"]}
-{"question": "Gene TCOF1 has a genetic association with diseases such as", "references": ["Treacher Collins syndrome", "mandibulofacial dysostosis", "Franceschetti syndrome", "(Mandibulofacial dysostosis) or (Franceschetti syndrome)", "Mandibulofacial dysostosis without limb anomalies", "Franceschetti-Klein syndrome"]}
-{"question": "Gene sickle-cell disease has a genetic association with diseases such as", "references": ["NPRL3", "C16orf35", "CGTHBA", "HS-40", "MARE", "NPR3", "RMD11", "NPR3 like, GATOR1 complex subunit", "FFEVF3", "BCL11A", "BCL11A-L", "BCL11A-S", "BCL11A-XL", "BCL11a-M", "CTIP1", "EVI9", "HBFQTL5", "ZNF856", "B-cell CLL/lymphoma 11A", "DILOS", "B cell CLL/lymphoma 11A", "BCL11A, BAF complex component", "BAF chromatin remodeling complex subunit BCL11A", "SMARCM1"]}
-{"question": "Gene NDE1 has a genetic association with diseases such as", "references": ["microhydranencephaly", "MHAC", "MICROHYDRANENCEPHALY; MHAC", "Hydranencephaly and Microcephaly", "MICROHYDRANENCEPHALY"]}
-{"question": "Gene ACAD10 has a genetic association with diseases such as", "references": ["esophageal cancer", "esophagus cancer", "oesophageal cancer", "cancer of the oesophagus", "malignant neoplasm of proximal third of esophagus", "malignant tumor of Proximal Third of esophagus", "Ca middle third oesophagus", "malignant neoplasm of distal third of esophagus", "malignant neoplasm of lower third of oesophagus", "Ca lower third oesophagus", "malignant tumor of the middle Third of the esophagus", "malignant neoplasm of upper third esophagus", "malignant tumor of abdominal esophagus", "malignant neoplasm of middle third of oesophagus", "malignant tumor of Distal Third of esophagus", "Malignant Neoplasm of the Abdominal Esophagus", "Malignant Tumor of the Abdominal Esophagus", "cancer of abdominal part of esophagus", "abdominal part of esophagus cancer", "malignant abdominal part of esophagus neoplasm", "malignant neoplasm of abdominal part of esophagus"]}
-{"question": "Gene SORL1 has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene ING3 has a genetic association with diseases such as", "references": ["head and neck squamous cell carcinoma", "HNSCC", "carcinoma of the head and neck", "squamous cell carcinoma of the head and neck", "squamous cell carcinomas of head and neck", "Head and neck squamous cell carcinoma", "SQUAMOUS CELL CARCINOMA, HEAD AND NECK; HNSCC", "Head and neck squamous cell carcinoma, NOS", "SCCHN", "craniocervical region squamous cell carcinoma", "SQUAMOUS CELL CARCINOMA, HEAD AND NECK", "Squamous Cell Carcinoma of Head and Neck"]}
-{"question": "Gene PEX13 has a genetic association with diseases such as", "references": ["Zellweger spectrum disorder", "Peroxisomal Biogenesis Disorders", "Zellweger Syndrome Spectrum", "Cerebrohepatorenal Syndrome", "ZSS", "Peroxisome biogenesis disorders-Zellweger spectrum disorders", "peroxisome biogenesis disorder", "peroxisome biogenesis disorders, Zellweger syndrome spectrum", "PBD-ZSD", "Zellweger syndrome spectrum", "Peroxisome biogenesis disorder spectrum", "ZSD", "Zellweger spectrum", "PBD, ZSS", "cerebrohepatorenal syndrome", "Zellweger spectrum disorder", "Peroxisome biogenesis disorder", "obsolete Zellweger spectrum disorder"]}
-{"question": "Gene ADAMTS6 has a genetic association with diseases such as", "references": ["osteosarcoma", "Osteogenic sarcoma", "Skeletal sarcoma", "osteoid sarcoma", "OSTEOSARCOMA, MALIGNANT", "sarcoma of osteoid"]}
-{"question": "Gene Nager acrofacial dysostosis has a genetic association with diseases such as", "references": ["SF3B4", "AFD1", "Hsh49", "SAP49", "SF3b49", "splicing factor 3b subunit 4"]}
-{"question": "Gene RADIL has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene TAGAP has a genetic association with diseases such as", "references": ["multiple sclerosis", "MS", "encephalomyelitis disseminata", "insular sclerosis", "disseminated sclerosis", "generalized multiple sclerosis", "Generalized multiple sclerosis (disorder)", "generalised multiple sclerosis", "Multiple sclerosis; MS", "Multiple sclerosis", "coeliac disease", "celiac sprue", "celiac disease", "nontropical sprue", "endemic sprue", "gluten enteropathy", "idiopathic steatorrhea", "CeD"]}
-{"question": "Gene McKusick\u2013Kaufman syndrome has a genetic association with diseases such as", "references": ["MKKS", "BBS6", "HMCS", "KMS", "MKS", "McKusick-Kaufman syndrome", "MKKS centrosomal shuttling protein"]}
-{"question": "Gene VPS33B has a genetic association with diseases such as", "references": ["Arthrogryposis\u2013renal dysfunction\u2013cholestasis syndrome", "ARC syndrome", "ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS", "Arthrogryposis, renal dysfunction and cholestasis (ARC) syndrome", "Arthrogryposis-renal dysfunction-cholestasis", "ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1; ARCS1", "Arthrogryposis, Renal Dysfunction, and Cholestasis type 1", "ARTHROGRYPOSIS, RENAL DYSFUNCTION, AND CHOLESTASIS 1", "ARCS1"]}
-{"question": "Gene HRAS has a genetic association with diseases such as", "references": ["Costello syndrome", "FCS SYNDROME", "Faciocutaneoskeletal Syndrome", "CSTLO", "COSTELLO SYNDROME", "Myopathy, Congenital, With Excess of Muscle Spindles", "COSTELLO SYNDROME; CSTLO", "follicular thyroid cancer", "follicular thyroid carcinoma", "Follicular adenocarcinoma (morphologic abnormality)", "Follicular adenocarcinoma, well differentiated (morphologic abnormality)", "Follicular carcinoma", "Follicular carcinoma of the Thyroid gland", "Follicular thyroid carcinoma (disorder)", "thyroid adenocarcinoma", "thyroid gland follicular carcinoma", "Follicular adenocarcinoma", "Follicular adenocarcinoma, well differentiated", "THYROID CANCER, NONMEDULLARY, 2; NMTC2", "THYROID CANCER, NONMEDULLARY, 2", "Thyroid Cancer, Nonmedullary, type 2", "NMTC2", "Adenocarcinoma, Follicular", "bladder cancer", "tumor of the bladder", "Malignant Tumor of Urinary Bladder", "Malignant Neoplasm, Urinary Bladder", "Malignant Urinary Bladder Tumor", "Malignant Tumor of Bladder", "cancer of urinary bladder", "Malignant Bladder Tumor", "Urinary Bladder Malignant Tumor", "Malignant Tumor, Urinary Bladder", "Malignant Tumor of the Bladder", "Malignant Bladder Neoplasm", "Malignant Urinary Bladder Neoplasm", "Malignant Neoplasm of the Urinary Bladder", "Malignant Neoplasm of Urinary Bladder", "Malignant Neoplasm of Bladder", "Malignant Neoplasm of the Bladder", "Urinary Bladder Malignant Neoplasm", "Malignant Tumor of the Urinary Bladder", "Malignant Neoplasm, Bladder", "urinary bladder cancer", "Schimmelpenning syndrome", "Linear nevus sebaceous syndrome (LNSS)", "Schimmelpenning-Feuerstein-Mims syndrome", "Feuerstein-Mims syndrome", "sebaceous nevus syndrome", "linear nevus sebaceous syndrome of Jadassohn", "Nevus sebaceus syndrome", "Solomon syndrome", "Jadassohn's nevus phakomatosis", "Nevus sebaceus of Jadassohn", "Organoid nevus syndrome", "Epidermal Nevus Syndrome, Formerly", "SFM syndrome", "Jadassohn nevus phakomatosis", "Organoid Nevus Phakomatosis", "Epidermal Nevus Syndrome", "Schimmelpenning Feuerstein Mims syndrome", "Linear nevus sebaceous syndrome", "Sebaceous nevus syndrome linear", "Schimmelpenning syndrome", "JNP", "Sebaceous Nevus Syndrome, Linear", "Linear Sebaceous Nevus Syndrome", "SFM", "SCHIMMELPENNING-FEUERSTEIN-MIMS SYNDROME; SFM", "linear nevus sebaceous syndrome"]}
-{"question": "Gene Cole-Carpenter syndrome has a genetic association with diseases such as", "references": ["SEC24D", "CLCRP2", "SEC24 homolog D, COPII coat complex component", "P4HB", "DSI", "ERBA2L", "GIT", "P4Hbeta", "PDI", "PDIA1", "PHDB", "PO4DB", "PO4HB", "PROHB", "CLCRP1", "prolyl 4-hydroxylase subunit beta"]}
-{"question": "Gene Haim\u2013Munk syndrome has a genetic association with diseases such as", "references": ["CTSC", "CPPI", "DPP-I", "DPP1", "DPPI", "HMS", "JP", "JPD", "PALS", "PDON1", "PLS", "cathepsin C"]}
-{"question": "Gene focal epilepsy has a genetic association with diseases such as", "references": ["ADCY9", "AC9", "ACIX", "adenylate cyclase 9", "ZNF385D", "ZNF659", "zinc finger protein 385D", "PTPRD", "HPTP", "HPTPD", "HPTPDELTA", "PTPD", "RPTPDELTA", "protein tyrosine phosphatase, receptor type D", "protein tyrosine phosphatase receptor type D", "R-PTP-delta"]}
-{"question": "Gene BMPR1A has a genetic association with diseases such as", "references": ["juvenile polyposis syndrome", "JUVENILE POLYPOSIS SYNDROME; JPS", "Juvenile Intestinal Polyposis", "Juvenile Polyposis of Stomach", "Polyposis, Familial, of Entire Gastrointestinal Tract", "JPS", "Polyposis, Juvenile Intestinal", "Juvenile Polyposis Coli", "JUVENILE POLYPOSIS SYNDROME", "juvenile polyp", "Retention Polyp", "Juvenile Polyp", "Juvenile Multiple Polyps Syndrome", "Juvenile Polyposis Syndrome", "Juvenile intestinal polyposis", "JIP", "Juvenile gastrointestinal polyposis", "Juvenile Polyposis"]}
-{"question": "Gene ETV5 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene rapadilino syndrome has a genetic association with diseases such as", "references": ["RECQL4", "RECQ4", "RecQ like helicase 4"]}
-{"question": "Gene SCN4A has a genetic association with diseases such as", "references": ["paramyotonia congenita", "PC", "paramyotonia congenita of von Eulenburg", "Eulenburg disease", "PMC", "Paramyotonia Congenita Without Cold Paralysis", "Paramyotonia congenita", "Paralysis Periodica Paramyotonica", "PARAMYOTONIA CONGENITA OF VON EULENBURG; PMC", "hypokalemic periodic paralysis", "Hypokalemic familial periodic paralysis", "Hypokalemic periodic paralysis (disorder)", "Periodic paralysis I", "familial hypokalemic periodic paralysis (disorder)", "familial periodic paralysis (& [hypokalaemic])", "periodic hypokalemic paralysis", "HOKPP", "familial periodic paralysis", "familial hypokalemic periodic paralysis", "Hypokalemic periodic paralysis", "Westphal disease", "hyperkalemic periodic paralysis", "familial hyperkalemic periodic paralysis (disorder)", "familial hyperkalemic periodic paralysis (disorder) [Ambiguous]", "hyperkalemic periodic paralysis (disorder)", "familial hyperkalemic periodic paralysis"]}
-{"question": "Gene Paget's disease of bone has a genetic association with diseases such as", "references": ["SQSTM1", "A170", "OSIL", "PDB3", "ZIP3", "p60", "p62", "p62B", "FTDALS3", "Sequestosome 1", "NADGP", "DMRV"]}
-{"question": "Gene congenital stromal corneal dystrophy has a genetic association with diseases such as", "references": ["DCN", "Dcn", "DC", "DSPG2", "PG40", "PGII", "PGS2", "SLRR1B", "mDcn", "CSCD", "decorin"]}
-{"question": "Gene EXT2 has a genetic association with diseases such as", "references": ["Potocki\u2013Shaffer syndrome", "Chromosome 11P11.2 Deletion Syndrome", "Proximal 11P Deletion Syndrome", "POTOCKI-SHAFFER SYNDROME", "11p11.2 deletion", "Pss", "Defect11 Syndrome", "Potocki-Shaffer syndrome"]}
-{"question": "Gene anterior segment mesenchymal dysgenesis has a genetic association with diseases such as", "references": ["PITX3", "ASMD", "ASOD", "CTPP4", "CTRCT11", "PTX3", "paired like homeodomain 3", "ASGD1"]}
-{"question": "Gene Marie Unna hereditary hypotrichosis has a genetic association with diseases such as", "references": ["HR", "ALUNC", "AU", "HSA277165", "HYPT4", "MUHH", "MUHH1", "hair growth associated", "HR, lysine demethylase and nuclear receptor corepressor", "HR lysine demethylase and nuclear receptor corepressor"]}
-{"question": "Gene VCAN has a genetic association with diseases such as", "references": ["Wagner's disease", "Wagner disease", "Erosive Vitreoretinopathy", "WGVRP", "Vitreoretinal degeneration, Wagner type", "WAGNER VITREORETINOPATHY", "WAGNER VITREORETINOPATHY; WGVRP", "Wagner Syndrome 1", "Wagner syndrome", "Hyaloideoretinal Degeneration of Wagner", "VCAN-related vitreoretinopathy", "Dominant hyaloideoretinal dystrophy of Wagner", "Wagner Vitreoretinal Degeneration"]}
-{"question": "Gene alcohol abuse has a genetic association with diseases such as", "references": ["ESRRG", "ERR3", "ERRgamma", "NR3B3", "estrogen related receptor gamma", "ERRg", "ERR-gamma", "ADH1B", "ADH2", "HEL-S-117", "alcohol dehydrogenase 1B (class I), beta polypeptide", "LMO1", "RBTN1", "RHOM1", "TTG1", "LIM domain only 1", "EXOC5", "HSEC10", "PRO1912", "SEC10", "SEC10L1", "SEC10P", "exocyst complex component 5", "KCNJ6", "BIR1", "GIRK-2", "GIRK2", "KATP-2", "KATP2", "KCNJ7", "KIR3.2", "hiGIRK2", "KPLBS", "potassium voltage-gated channel subfamily J member 6", "potassium inwardly rectifying channel subfamily J member 6", "RIPOR2", "C6orf32", "DIFF40", "DIFF48", "MYONAP", "PL48", "FAM65B", "DFNB104", "family with sequence similarity 65 member B", "RHO family interacting cell polarization regulator 2", "HIP1", "HIP-I", "ILWEQ", "SHON", "SHONbeta", "SHONgamma", "huntingtin interacting protein 1", "MBNL2", "MBLL", "MBLL39", "PRO2032", "muscleblind like splicing regulator 2", "DCC", "DCC netrin 1 receptor", "CRC18", "CRCR1", "IGDCC1", "MRMV1", "NTN1R1", "HGPPS2", "C15orf32", "chromosome 15 open reading frame 32", "chromosome 15 putative open reading frame 32", "AUTS2", "FBRSL2", "MRD26", "AUTS2, activator of transcription and developmental regulator", "activator of transcription and developmental regulator AUTS2", "OAS3", "p100", "p100OAS", "2'-5'-oligoadenylate synthetase 3"]}
-{"question": "Gene Limb\u2013mammary syndrome has a genetic association with diseases such as", "references": ["TP63", "AIS", "B(p51A)", "B(p51B)", "EEC3", "KET", "LMS", "NBP", "OFC8", "RHS", "SHFM4", "TP53CP", "TP53L", "TP73L", "p40", "p51", "p53CP", "p63", "p73H", "p73L", "tumor protein p63"]}
-{"question": "Gene STAT3 has a genetic association with diseases such as", "references": ["Crohn's disease", "regional enteritis", "Crohn disease", "Crohn's disease of colon (disorder)", "Crohn's disease of large bowel", "Granulomatous Colitis", "regional Ileitis", "regional colitis", "regional enteritis of small intestine with large intestine", "regional enteritis of the large bowel", "regional ileocolitis", "Crohn's disease of colon", "Crohn", "multiple sclerosis", "MS", "encephalomyelitis disseminata", "insular sclerosis", "disseminated sclerosis", "generalized multiple sclerosis", "Generalized multiple sclerosis (disorder)", "generalised multiple sclerosis", "Multiple sclerosis; MS", "Multiple sclerosis"]}
-{"question": "Gene Wiedemann-Steiner syndrome has a genetic association with diseases such as", "references": ["KMT2A", "ALL-1", "CXXC7", "HRX", "HTRX1", "MLL", "MLL/GAS7", "MLL1", "MLL1A", "TET1-MLL", "TRX1", "WDSTS", "MLL-AF9", "lysine methyltransferase 2A", "Histone-lysine N-methyltransferase HRX"]}
-{"question": "Gene hereditary hemorrhagic telangiectasia has a genetic association with diseases such as", "references": ["ENG", "Eng", "AI528660", "AI662476", "CD105", "Endo", "S-endoglin", "END", "HHT1", "ORW1", "endoglin", "ACVRL1", "ACVRLK1", "ALK-1", "ALK1", "HHT", "HHT2", "ORW2", "SKR3", "TSR-I", "activin A receptor like type 1", "GDF2", "BMP-9", "BMP9", "HHT5", "growth differentiation factor 2"]}
-{"question": "Gene AP1S2 has a genetic association with diseases such as", "references": ["X-linked intellectual disability", "syndromic X-linked intellectual disability", "syndromic X-linked mental retardation", "syndromic intellectual disability, X-linked", "Mental Retardation, X-Linked"]}
-{"question": "Gene DCDC2 has a genetic association with diseases such as", "references": ["ciliopathy", "ciliopathies"]}
-{"question": "Gene mucolipidosis type IV has a genetic association with diseases such as", "references": ["MCOLN1", "MG-2", "ML4", "MLIV", "MST080", "MSTP080", "TRP-ML1", "TRPM-L1", "TRPML1", "mucolipin 1", "ML1", "mucolipin TRP cation channel 1"]}
-{"question": "Gene PABPN1 has a genetic association with diseases such as", "references": ["oculopharyngeal muscular dystrophy", "Muscular dystrophy, oculopharyngeal", "Oculopharyngeal muscular dystrophy (disorder)", "OPMD", "Oculopharyngeal muscular dystrophy", "OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OPMD"]}
-{"question": "Gene PAX4 has a genetic association with diseases such as", "references": ["type-1 diabetes", "IDDM", "insulin-dependent diabetes mellitus", "type I diabetes mellitus", "T1DM", "insulin dependent diabetes", "juvenile diabetes", "diabetes mellitus juvenile type", "DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM", "Diabetes Mellitus, Type 1", "Diabetes Mellitus, Insulin-Dependent, 1", "DIABETES MELLITUS, INSULIN-DEPENDENT", "Juvenile-Onset Diabetes", "Insulin-Dependent Diabetes Mellitus 1", "diabetes (type 1)", "type 1 diabetes mellitus"]}
-{"question": "Gene FRAS1 has a genetic association with diseases such as", "references": ["Fraser syndrome", "cryptophthalmos with other malformations", "Ulrich-Feichtiger syndrome", "Cryptophthalmos-Syndactyly Syndrome", "Cyclopism", "Cryptophthalmos syndrome", "Meyer-Schwickerath's syndrome", "FRASER SYNDROME", "Fraser-Francois syndrome"]}
-{"question": "Gene NXPH1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene fucosidosis has a genetic association with diseases such as", "references": ["FUCA1", "FUCA", "fucosidase, alpha-L- 1, tissue", "alpha-L-fucosidase 1"]}
-{"question": "Gene SLC4A7 has a genetic association with diseases such as", "references": ["breast cancer", "malignant neoplasm of breast", "malignant tumor of the breast", "mammary cancer", "primary breast cancer", "breast disorder"]}
-{"question": "Gene EXOC1 has a genetic association with diseases such as", "references": ["cervical cancer", "cervix cancer", "cervix uteri cancer", "tumor of the Cervix Uteri", "malignant neoplasm of uterine cervix", "Malignant Uterine Cervix Neoplasm", "Malignant Neoplasm of the Cervix", "Malignant Cervix Uteri Tumor", "Malignant Cervix Tumor", "Malignant Neoplasm of Cervix", "Malignant Tumor of the Uterine Cervix", "Malignant Tumor of the Cervix", "Malignant Tumor of the Cervix Uteri", "Malignant Cervical Tumor", "Malignant Uterine Cervix Tumor", "Malignant Tumor of Uterine Cervix", "Malignant Cervix Uteri Neoplasm", "cancer of uterine cervix", "uterine cervix cancer", "Malignant Cervix Neoplasm", "Malignant Tumor of Cervix", "Malignant Neoplasm of the Uterine Cervix", "Malignant Tumor of Cervix Uteri", "Malignant Neoplasm of Cervix Uteri", "Malignant Cervical Neoplasm", "Malignant Neoplasm of the Cervix Uteri"]}
-{"question": "Gene autosomal recessive ataxia, Beauce type has a genetic association with diseases such as", "references": ["SYNE1", "8B", "ARCA1", "C6orf98", "CPG2", "EDMD4", "MYNE1", "Nesp1", "SCAR8", "dJ45H2.2", "spectrin repeat containing nuclear envelope protein 1", "KASH1", "AMCM", "AMC3"]}
-{"question": "Gene LINGO1 has a genetic association with diseases such as", "references": ["essential tremor", "ET", "benign tremor", "familiar tremor", "benign essential tremor", "essential hereditary tremor", "shaky hand syndrome"]}
-{"question": "Gene spermatogenesis arrest has a genetic association with diseases such as", "references": ["SYCP3", "COR1", "SCP3", "SPGF4", "RPRGL4", "synaptonemal complex protein 3"]}
-{"question": "Gene RIT1 has a genetic association with diseases such as", "references": ["conduct disorder", "disruptive behavior disorder"]}
-{"question": "Gene OTUD7B has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene drusen has a genetic association with diseases such as", "references": ["EFEMP1", "DHRD", "DRAD", "FBLN3", "FBNL", "FIBL-3", "MLVT", "MTLV", "S1-5", "EGF containing fibulin like extracellular matrix protein 1", "EGF containing fibulin extracellular matrix protein 1"]}
-{"question": "Gene DCTD has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene toxic diffuse goiter has a genetic association with diseases such as", "references": ["SLAMF6", "CD352", "KALI", "KALIb", "Ly108", "NTB-A", "NTBA", "SF2000", "SLAM family member 6", "ABO", "A3GALNT", "A3GALT1", "GTB", "NAGAT", "ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase)", "ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase", "FCRL3", "CD307c", "FCRH3", "IFGP3", "IRTA3", "SPAP2", "Fc receptor like 3"]}
-{"question": "Gene MTNR1B has a genetic association with diseases such as", "references": ["type 2 diabetes", "NIDDM", "non-insulin-dependent diabetes mellitus", "type II diabetes mellitus", "Diabetes mellitus type 2", "Rare insulin-independent diabetes mellitus", "Diabetes Mellitus, Type 2", "type 2 diabetes mellitus", "diabetes (type 2)"]}
-{"question": "Gene cardiac arrest has a genetic association with diseases such as", "references": ["AKAP10", "AKAP-10", "D-AKAP-2", "D-AKAP2", "PRKA10", "A-kinase anchoring protein 10"]}
-{"question": "Gene RTKN2 has a genetic association with diseases such as", "references": ["rheumatoid arthritis", "Arthritis or polyarthritis, rheumatic", "atrophic Arthritis", "Rheumatoid arthritis with vasculitis", "Malignant rheumatoid arthritis", "Rheumatoid arthritis"]}
-{"question": "Gene chronic lymphocytic leukemia has a genetic association with diseases such as", "references": ["CAMK2D", "CAMKD", "calcium/calmodulin dependent protein kinase II delta", "CLPTM1L", "CRR9", "CLPTM1-like", "CLPTM1 like", "POT1", "CMM10", "HPOT1", "GLM9", "protection of telomeres 1", "IRF4", "LSIRF", "MUM1", "NF-EM5", "SHEP8", "interferon regulatory factor 4", "BAK1", "BAK", "BAK-LIKE", "BCL2L7", "CDN1", "BCL2 antagonist/killer 1", "IRF8", "H-ICSBP", "ICSBP", "ICSBP1", "IMD32A", "IMD32B", "IRF-8", "interferon regulatory factor 8", "LEF1", "LEF-1", "TCF10", "TCF1ALPHA", "TCF7L3", "lymphoid enhancer binding factor 1", "FARP2", "FIR", "FRG", "PLEKHC3", "FERM, ARH/RhoGEF and pleckstrin domain protein 2", "HLA-DQA1", "CD", "CELIAC1", "DQ-A1", "GSE", "HLA-DQA", "Major histocompatibility complex, class II, DQ alpha 1", "DQA1", "GRAMD1B", "GRAM domain containing 1B", "LINC01059", "Aster-B", "ARL11", "ARLTS1", "ADP ribosylation factor like GTPase 11"]}
-{"question": "Gene FGFR3 has a genetic association with diseases such as", "references": ["Crouzonodermoskeletal syndrome", "Crouzon syndrome-acanthosis nigricans syndrome", "Crouzonodermoskeletal syndrome", "Crouzon-dermoskeletal syndrome", "CAN", "CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS", "CROUZON SYNDROME WITH ACANTHOSIS NIGRICANS; CAN", "bladder cancer", "tumor of the bladder", "Malignant Tumor of Urinary Bladder", "Malignant Neoplasm, Urinary Bladder", "Malignant Urinary Bladder Tumor", "Malignant Tumor of Bladder", "cancer of urinary bladder", "Malignant Bladder Tumor", "Urinary Bladder Malignant Tumor", "Malignant Tumor, Urinary Bladder", "Malignant Tumor of the Bladder", "Malignant Bladder Neoplasm", "Malignant Urinary Bladder Neoplasm", "Malignant Neoplasm of the Urinary Bladder", "Malignant Neoplasm of Urinary Bladder", "Malignant Neoplasm of Bladder", "Malignant Neoplasm of the Bladder", "Urinary Bladder Malignant Neoplasm", "Malignant Tumor of the Urinary Bladder", "Malignant Neoplasm, Bladder", "urinary bladder cancer", "Muenke syndrome", "Muenke Syndrome", "FGFR3-related craniosynostosis", "Muenke Nonsyndromic Coronal Craniosynostosis", "MNKES", "Syndrome of coronal craniosynostosis", "MUENKE SYNDROME; MNKES", "seborrheic keratosis", "Keratosis Seborrheica", "Basal Cell Papilloma", "Keratosis, Seborrheic", "SADDAN", "Severe Achondroplasia with Developmental Delay and Acanthosis Nigricans", "severe achondroplasia with developmental delay and acanthosis nigricans", "SADDAN dysplasia", "ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS; SADDAN", "SADDAN", "ACHONDROPLASIA, SEVERE, WITH DEVELOPMENTAL DELAY AND ACANTHOSIS NIGRICANS"]}
-{"question": "Gene TLR3 has a genetic association with diseases such as", "references": ["herpesviral encephalitis", "Herpes simplex virus encephalitis", "Encephalopathy, Acute, Infection-Induced, Susceptibility To, 2", "HERPES SIMPLEX ENCEPHALITIS, SUSCEPTIBILITY TO, 2", "Herpes Simplex Encephalitis, Susceptibility To, type 2", "obsolete Herpes simplex virus encephalitis"]}
-{"question": "Gene GDF1 has a genetic association with diseases such as", "references": ["tetralogy of Fallot", "Ventricular septal defect with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle", "TOF", "Fallot tetralogy", "TETRALOGY OF FALLOT", "TETRALOGY OF FALLOT; TOF"]}
-{"question": "Gene LTBP1 has a genetic association with diseases such as", "references": ["smallpox", "ordinary smallpox", "variola", "variola vera"]}
-{"question": "Gene FUT2 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "Crohn's disease", "regional enteritis", "Crohn disease", "Crohn's disease of colon (disorder)", "Crohn's disease of large bowel", "Granulomatous Colitis", "regional Ileitis", "regional colitis", "regional enteritis of small intestine with large intestine", "regional enteritis of the large bowel", "regional ileocolitis", "Crohn's disease of colon", "Crohn"]}
-{"question": "Gene PEX1 has a genetic association with diseases such as", "references": ["Zellweger spectrum disorder", "Peroxisomal Biogenesis Disorders", "Zellweger Syndrome Spectrum", "Cerebrohepatorenal Syndrome", "ZSS", "Peroxisome biogenesis disorders-Zellweger spectrum disorders", "peroxisome biogenesis disorder", "peroxisome biogenesis disorders, Zellweger syndrome spectrum", "PBD-ZSD", "Zellweger syndrome spectrum", "Peroxisome biogenesis disorder spectrum", "ZSD", "Zellweger spectrum", "PBD, ZSS", "cerebrohepatorenal syndrome", "Zellweger spectrum disorder", "Peroxisome biogenesis disorder", "obsolete Zellweger spectrum disorder"]}
-{"question": "Gene Reis-B\u00fccklers corneal dystrophy has a genetic association with diseases such as", "references": ["TGFBI", "BIGH3", "CDB1", "CDG2", "CDGG1", "CSD", "CSD1", "CSD2", "CSD3", "EBMD", "LCD1", "transforming growth factor beta induced"]}
-{"question": "Gene CYLD has a genetic association with diseases such as", "references": ["Multiple familial trichoepithelioma", "TRICHOEPITHELIOMA, MULTIPLE FAMILIAL, 1", "Epithelioma, Hereditary Multiple Benign Cystic", "Mft1", "Epithelioma Adenoides Cysticum of Brooke", "Trichoepithelioma, Multiple Familial, type 1", "Brooke-Fordyce Trichoepitheliomas"]}
-{"question": "Gene myelodysplastic syndrome has a genetic association with diseases such as", "references": ["ASXL1", "BOPS", "MDS", "additional sex combs like 1, transcriptional regulator", "ASXL transcriptional regulator 1", "SETBP1", "SET binding protein 1", "SEB", "MRD29", "SET bindign protein 1", "TET2", "KIAA1546", "MDS", "tet methylcytosine dioxygenase 2", "Tet methylcytosine dioxygenase 2", "IMD75", "GATA2", "DCML", "IMD21", "MONOMAC", "NFE1B", "GATA binding protein 2"]}
-{"question": "Gene cleft lip and cleft palate has a genetic association with diseases such as", "references": ["IRF6", "LPS", "OFC6", "PIT", "PPS", "PPS1", "VWS", "VWS1", "interferon regulatory factor 6", "PAX7", "HUP1", "PAX7B", "RMS2", "Pax7", "paired box 7", "MYOSCO", "THADA", "GITA", "ARMC13", "THADA, armadillo repeat containing", "THADA armadillo repeat containing", "FHIT", "AP3Aase", "FRA3B", "fragile histidine triad", "tr\u00edada histidina fr\u00e0gil", "fragile histidine triad diadenosine triphosphatase", "LRRC7", "DENSIN", "leucine rich repeat containing 7", "SPATA13", "ARHGEF29", "ASEF2", "spermatogenesis associated 13", "SH3BP4", "BOG25", "TTP", "SH3 domain binding protein 4", "RASGRF2", "GRF2", "RAS-GRF2", "Ras protein specific guanine nucleotide releasing factor 2", "ATXN3", "AT3", "ATX3", "JOS", "MJD", "MJD1", "SCA3", "Ataxin 3", "BMP6", "VGR", "VGR1", "bone morphogenetic protein 6", "BMP4", "BMP2B", "BMP2B1", "MCOPS6", "OFC11", "ZYME", "bone morphogenetic protein 4", "SUMO1", "DAP1", "GMP1", "OFC10", "PIC1", "SENP2", "SMT3", "SMT3C", "SMT3H3", "UBL1", "small ubiquitin-like modifier 1", "small ubiquitin like modifier 1", "MSX1", "ECTD3", "HOX7", "HYD1", "STHAG1", "msh homeobox 1"]}
-{"question": "Gene facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation has a genetic association with diseases such as", "references": ["WAC", "BM-016", "PRO1741", "Wwp4", "DESSH", "WW domain containing adaptor with coiled-coil"]}
-{"question": "Gene GALNT2 has a genetic association with diseases such as", "references": ["metabolic disease", "metabolic illness", "disorder of metabolic process", "metabolic disorder", "metabolic diseases", "disease of metabolism"]}
-{"question": "Gene GSDMB has a genetic association with diseases such as", "references": ["asthma", "exercise-induced asthma", "chronic obstructive asthma", "chronic obstructive asthma with status asthmaticus", "chronic obstructive asthma with acute exacerbation", "bronchial hyperreactivity", "Exercise induced asthma", "Asthma", "asthma brionchiole"]}
-{"question": "Gene amelogenesis imperfecta type 1G has a genetic association with diseases such as", "references": ["FAM20A", "AI1G", "AIGFS", "FP2747", "family with sequence similarity 20 member A", "FAM20A, golgi associated secretory pathway pseudokinase", "FAM20A golgi associated secretory pathway pseudokinase"]}
-{"question": "Gene 3-methylglutaconic aciduria type 3 has a genetic association with diseases such as", "references": ["OPA3", "MGA3", "optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)", "OPA3, outer mitochondrial membrane lipid metabolism regulator", "OPA3 outer mitochondrial membrane lipid metabolism regulator", "outer mitochondrial membrane lipid metabolism regulator OPA3"]}
-{"question": "Gene polydactyly has a genetic association with diseases such as", "references": ["LMBR1", "ACHP", "C7orf2", "DIF14", "PPD2", "TPT", "ZRS", "LSS", "THYP", "limb development membrane protein 1", "GLI3", "ACLS", "GCPS", "GLI3-190", "GLI3FL", "PAP-A", "PAPA", "PAPA1", "PAPB", "PHS", "PPDIV", "GLI family zinc finger 3"]}
-{"question": "Gene generalized epilepsy with febrile seizures plus has a genetic association with diseases such as", "references": ["SCN1B", "ATFB13", "BRGDA5", "GEFSP1", "sodium voltage-gated channel beta subunit 1", "EIEE52", "DEE52", "SCN1A", "EIEE6", "FEB3", "FEB3A", "FHM3", "GEFSP2", "HBSCI", "NAC1", "Nav1.1", "SCN1", "SMEI", "sodium voltage-gated channel alpha subunit 1", "DRVT", "DEE6", "DEE6A", "DEE6B", "SCN9A", "ETHA", "FEB3B", "GEFSP7", "HSAN2D", "NE-NA", "NENA", "Nav1.7", "PN1", "SFNP", "sodium voltage-gated channel alpha subunit 9", "GABRG2", "CAE2", "ECA2", "GEFSP3", "gamma-aminobutyric acid type A receptor gamma2 subunit", "EIEE74", "FEB8"]}
-{"question": "Gene TRIP4 has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene Gerstmann-Straussler-Scheinker syndrome has a genetic association with diseases such as", "references": ["PRNP", "ASCR", "AltPrP", "CD230", "CJD", "GSS", "KURU", "PRIP", "PrP", "PrP27-30", "PrP33-35C", "PrPc", "p27-30", "prion protein"]}
-{"question": "Gene SLC1A1 has a genetic association with diseases such as", "references": ["schizophrenia", "Morel-Kraepelin disease", "Kraepelin-Morel disease", "dementia pr\u00e6cox", "dementia praecox", "schizophrenia-1", "dicarboxylic aminoaciduria", "glutamate-aspartate transport defect", "Dicarboxylicaminoaciduria", "DCBXA", "DICARBOXYLIC AMINOACIDURIA; DCBXA", "DICARBOXYLIC AMINOACIDURIA"]}
-{"question": "Gene TFDP2 has a genetic association with diseases such as", "references": ["kidney disease", "renal disease", "kidney damage", "kidney injury", "nephropathy", "disease of kidney", "disorder of kidney", "kidney necrosis", "nephron damage", "kidney diseases"]}
-{"question": "Gene ABCG8 has a genetic association with diseases such as", "references": ["sitosterolemia", "phytosterolemia", "SITOSTEROLEMIA", "Stsl", "Plant sterol storage disease", "Retention of dietary cholesterol and abnormal retention of non-cholesterol sterols in the body", "Macrothrombocytopenia/Stomatocytosis, Mediterranean"]}
-{"question": "Gene tetralogy of Fallot has a genetic association with diseases such as", "references": ["NRP1", "BDCA4", "CD304", "NP1", "NRP", "VEGF165R", "Neuropilin 1", "GPC5", "glypican 5", "JAG1", "Jag1", "ABE2", "Gsfabe2", "Htu", "Ozz", "Ser-1", "AGS", "AHD", "AWS", "CD339", "HJ1", "JAGL1", "jagged 1", "AGS1", "DCHE", "jagged canonical Notch ligand 1", "CMT2HH", "GATA4", "GATA binding protein 4", "ASD2", "TACHD", "VSD1", "TOF", "NKX2-5", "CHNG5", "CSX", "CSX1", "HLHS2", "NKX2.5", "NKX2E", "NKX4-1", "VSD3", "NK2 homeobox 5", "ZFPM2", "DIH3", "FOG2", "ZC2HC11B", "ZNF89B", "hFOG-2", "SRXY9", "zinc finger protein, FOG family member 2", "GATA6", "GATA binding protein 6", "GDF1", "DORV", "DTGA3", "RAI", "growth differentiation factor 1", "CHTD6", "UOG1", "LASS1", "CERS1", "LAG1", "TBX1", "CAFS", "CATCH22", "CTHM", "DGCR", "DGS", "DORV", "TBX1C", "TGA", "VCF", "VCFS", "T-box 1", "T-box transcription factor 1"]}
-{"question": "Gene TSLP has a genetic association with diseases such as", "references": ["allergic rhinitis", "allergic rhinitis due to animal (cat) (dog) hair and dander", "allergic rhinitis due to food", "atopic rhinitis", "pollenosis", "Allergic rhinitis due to pollen", "Allergic rhinitis due to pollen (disorder)", "Allergy to pollen (disorder)", "Hay fever - pollens", "Non-seasonal allergic rhinitis", "Perenial allergic rhinitis", "Pollinosis", "hfcy", "Rhinitis, Allergic"]}
-{"question": "Gene CEP164 has a genetic association with diseases such as", "references": ["ciliopathy", "ciliopathies"]}
-{"question": "Gene ATP2B1 has a genetic association with diseases such as", "references": ["coronary artery disease", "CAD", "atherosclerotic heart disease", "coronary heart disease", "ischemic heart disease", "IHD", "atherosclerotic cardiovascular disease", "CHD (coronary heart disease)", "coronary arteriosclerosis", "CHD", "coronary artery arteriosclerosis (disease)", "atherosclerosis of coronary artery", "Coronary Atherosclerosis", "arterial hypertension", "high blood pressure", "\"the silent killer\"", "hypertension"]}
-{"question": "Gene MEGF10 has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene TET2 has a genetic association with diseases such as", "references": ["breast cancer", "malignant neoplasm of breast", "malignant tumor of the breast", "mammary cancer", "primary breast cancer", "breast disorder", "melanoma", "malignant melanoma", "Naevocarcinom", "Naevocarcinoma", "MELANOMA, MALIGNANT", "Melanoma", "polycythemia vera", "Osler-Vaquez syndrome", "PV", "erythremia (morphologic abnormality)", "polycythaemia rubra vera", "proliferative polycythaemia", "Polycythemia Rubra Vera", "POLYCYTHEMIA VERA; PV", "Vaquez disease", "Polycythemia vera", "Osler-Vaquez disease", "Acquired primary erythrocytosis", "myelodysplastic syndrome", "preleukemia", "MDS", "Myelodysplastic syndrome, NOS", "Myelodysplastic Syndrome, Susceptibility to", "Dysmyelopoietic Syndrome", "Myelodysplasia", "MYELODYSPLASTIC SYNDROME", "myelodysplastic syndromes", "smoldering leukemia", "Oligoblastic Leukemia", "Myelodysplastic Neoplasm", "MYELODYSPLASTIC SYNDROME; MDS", "Hematopoeitic - Myelodysplastic Syndrome (MDS)", "Myelodysplastic Syndrome/Neoplasm"]}
-{"question": "Gene ZNF365 has a genetic association with diseases such as", "references": ["narcolepsy", "paroxysmal sleep", "Narcolepsy, without cataplexy", "Narcolepsy", "breast cancer", "malignant neoplasm of breast", "malignant tumor of the breast", "mammary cancer", "primary breast cancer", "breast disorder", "atopic dermatitis", "Allergic (intrinsic) eczema (disorder)", "Atopic dermatitis", "Atopic dermatitis (disorder)", "Atopic dermatitis NOS (disorder)", "Atopic neurodermatitis (disorder)", "Besnier's prurigo", "Besnier's prurigo (disorder)", "allergic dermatitis", "atopic eczema", "atopic dermatitis and related conditions", "Atopic neurodermatitis", "Allergic"]}
-{"question": "Gene Xia-Gibbs Syndrome has a genetic association with diseases such as", "references": ["AHDC1", "MRD25", "AT-hook DNA binding motif containing 1", "XIGIS"]}
-{"question": "Gene acute interstitial pneumonitis has a genetic association with diseases such as", "references": ["SFTPA2", "COLEC5", "PSAP", "PSP-A", "PSPA", "SFTP1", "SFTPA2B", "SP-A", "SPA2", "SPAII", "surfactant protein A2", "SP-2A", "ILD2"]}
-{"question": "Gene EMG1 has a genetic association with diseases such as", "references": ["Bowen-Conradi syndrome", "BOWEN-CONRADI SYNDROME", "Bowen Hutterite Syndrome, Formerly", "Bowen Hutterite Syndrome", "BOWEN-CONRADI SYNDROME; BWCNS", "BWCNS", "Bowen-Conradi Hutterite syndrome", "Bowen syndrome, Hutterite type", "Bowen Hutterite syndrome (formerly)"]}
-{"question": "Gene Potocki\u2013Shaffer syndrome has a genetic association with diseases such as", "references": ["ALX4", "CRS5", "FND2", "ALX homeobox 4", "EXT2", "SOTV", "SSMS", "exostosin glycosyltransferase 2"]}
-{"question": "Gene B3GLCT has a genetic association with diseases such as", "references": ["Peters plus syndrome", "Peters-plus syndrome", "Krause-Kivlin syndrome", "Peters anomaly-short limb dwarfism syndrome", "Peters anomaly with short limb dwarfism", "Peters Anomaly With Short-Limb Dwarfism", "Krause-van Schooneveld-Kivlin syndrome", "obsolete Peters-Plus Syndrome"]}
-{"question": "Gene UGT2B7 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene RFT1 has a genetic association with diseases such as", "references": ["smallpox", "ordinary smallpox", "variola", "variola vera"]}
-{"question": "Gene Hennekam syndrome has a genetic association with diseases such as", "references": ["CCBE1", "HKLLS1", "collagen and calcium binding EGF domains 1", "FAT4", "CDHF14", "CDHR11", "FAT-J", "FATJ", "NBLA00548", "VMLDS2", "HKLLS2", "FAT atypical cadherin 4"]}
-{"question": "Gene pulmonary emphysema has a genetic association with diseases such as", "references": ["BICD1", "BICD", "BICD cargo adaptor 1", "bic-D 1", "ADARB2", "ADAR3", "RED2", "adenosine deaminase, RNA specific B2 (inactive)", "adenosine deaminase RNA specific B2 (inactive)"]}
-{"question": "Gene IMMP2L has a genetic association with diseases such as", "references": ["Tourette syndrome", "Guinon's disease", "motor-verbal tic disorder", "Tourette's syndrome", "Chronic Motor Tics", "Tourette Disorder", "GTS", "psychogenic tics", "Gilles de la Tourette syndrome"]}
-{"question": "Gene monilethrix has a genetic association with diseases such as", "references": ["KRT86", "HB6", "Hb1", "KRTHB1", "KRTHB6", "MNX", "hHb6", "K86", "keratin 86", "KRT83", "HB3", "Hb-3", "KRTHB3", "keratin 83", "MNLIX", "EKVP5", "KRT81", "HB1", "Hb-1", "KRTHB1", "MLN137", "ghHkb1", "hHAKB2-1", "keratin 81", "K81"]}
-{"question": "Gene PKLR has a genetic association with diseases such as", "references": ["Pyruvate kinase deficiency", "pyruvate kinase deficiency of red cells", "hemolytic anemia due to red cell pyruvate kinase deficiency", "PK deficiency", "pyruvate kinase deficiency of erythrocyte", "Pyruvate kinase deficiency of erythrocytes"]}
-{"question": "Gene DHTKD1 has a genetic association with diseases such as", "references": ["Alpha-aminoadipic and alpha-ketoadipic aciduria", "2-aminoadipic 2-oxoadipic aciduria", "2-AMINOADIPIC 2-OXOADIPIC ACIDURIA; AMOXAD", "2-AMINOADIPIC 2-OXOADIPIC ACIDURIA", "Alpha-aminoadipic aciduria", "AMOXAD"]}
-{"question": "Gene IRF5 has a genetic association with diseases such as", "references": ["rheumatoid arthritis", "Arthritis or polyarthritis, rheumatic", "atrophic Arthritis", "Rheumatoid arthritis with vasculitis", "Malignant rheumatoid arthritis", "Rheumatoid arthritis"]}
-{"question": "Gene GSDMA has a genetic association with diseases such as", "references": ["asthma", "exercise-induced asthma", "chronic obstructive asthma", "chronic obstructive asthma with status asthmaticus", "chronic obstructive asthma with acute exacerbation", "bronchial hyperreactivity", "Exercise induced asthma", "Asthma", "asthma brionchiole"]}
-{"question": "Gene prostate cancer has a genetic association with diseases such as", "references": ["MSMB", "HPC13", "IGBF", "MSP", "MSPB", "PN44", "PRPS", "PSP", "PSP-94", "PSP57", "PSP94", "microseminoprotein, beta-", "microseminoprotein beta", "CEP152", "MCPH4", "MCPH9", "SCKL5", "centrosomal protein 152", "UPF2", "HUPF2", "RENT2", "smg-3", "UPF2 regulator of nonsense transcripts homolog (yeast)", "UPF2, regulator of nonsense mediated mRNA decay", "UPF2 regulator of nonsense mediated mRNA decay", "BAIAP2L1", "IRTKS", "BAI1 associated protein 2 like 1", "BAR/IMD domain containing adaptor protein 2 like 1", "ANK2", "ANK-2", "LQT4", "brank-2", "ankyrin 2, neuronal", "ankyrin 2", "TSEN2", "PCH2B", "SEN2", "SEN2L", "tRNA splicing endonuclease subunit 2", "EVC", "DWF-1", "EVC1", "EVCL", "EvC ciliary complex subunit 1", "TNRC6B", "trinucleotide repeat containing 6B", "trinucleotide repeat containing adaptor 6B", "GDSBA", "ANXA13", "ANX13", "ISA", "annexin A13", "ABLIM1", "ABLIM", "LIMAB1", "LIMATIN", "abLIM-1", "actin binding LIM protein 1", "TMTC2", "IBDBP1", "transmembrane and tetratricopeptide repeat containing 2", "transmembrane O-mannosyltransferase targeting cadherins 2", "TNC", "150-225", "DFNA56", "GMEM", "GP", "HXB", "JI", "TN", "TN-C", "Tenascin C", "ZNF280B", "5'OY11.1", "D87009.C22.3", "SUHW2", "ZNF279", "ZNF632", "zinc finger protein 280B", "EPHA10", "EPH receptor A10", "KIF13A", "RBKIN", "bA500C11.2", "kinesin family member 13A", "TERT", "CMM9", "DKCA2", "DKCB4", "EST2", "PFBMFT1", "TCS1", "TP2", "TRT", "hEST2", "hTRT", "telomerase reverse transcriptase", "HTERT", "FGF10", "fibroblast growth factor 10", "CCHCR1", "C6orf18", "HCR", "SBP", "coiled-coil alpha-helical rod protein 1", "pg8", "MLPH", "SLAC2-A", "melanophilin", "BIK", "BIP1", "BP4", "NBK", "BCL2 interacting killer", "FSHR", "FSHR1", "FSHRO", "LGR1", "ODG1", "follicle stimulating hormone receptor", "TTC7A", "MINAT", "TTC7", "GIDID", "tetratricopeptide repeat domain 7A", "PTGFRN", "CD315", "CD9P-1", "EWI-F", "FPRP", "SMAP-6", "prostaglandin F2 receptor inhibitor", "LRP1B", "LRP-DIT", "LRPDIT", "LDL receptor related protein 1B", "LRP-1B", "AOPEP", "chromosome 9 open reading frame 3", "AP-O", "APO", "C90RF3", "ONPEP", "aminopeptidase O (putative)", "C9orf3", "GLI2", "CJS", "HPE9", "PHS2", "THP1", "THP2", "GLI family zinc finger 2", "CNNM3", "ACDP3", "cyclin and CBS domain divalent metal cation transport mediator 3", "FOXP4", "hFKHLA", "forkhead box P4", "THADA", "GITA", "ARMC13", "THADA, armadillo repeat containing", "THADA armadillo repeat containing", "PDLIM5", "ENH", "ENH1", "LIM", "L9", "PDZ and LIM domain 5", "SLC22A3", "EMT", "EMTH", "OCT3", "solute carrier family 22 member 3", "LMTK2", "AATYK2", "BREK", "KPI-2", "KPI2", "LMR2", "PPP1R100", "cprk", "hBREK", "lemur tyrosine kinase 2", "CTBP2", "C-terminal binding protein 2", "JAZF1", "TIP27", "ZNF802", "JAZF zinc finger 1", "CTDSPL", "C3orf8", "HYA22", "PSR1", "RBSP3", "SCP3", "CTD small phosphatase like", "HAPLN1", "CRTL1", "CRT1", "hyaluronan and proteoglycan link protein 1", "RNASEL", "PRCA1", "RNS4", "ribonuclease L"]}
-{"question": "Gene GCSH has a genetic association with diseases such as", "references": ["glycine encephalopathy", "Non-ketotic hyperglycinemia", "Non-ketotic hyperglycinemia (disorder)", "nonketotic hyperglycinemia", "Glycine synthase deficiency", "Hyperglycinemia, Transient Neonatal", "GLYCINE ENCEPHALOPATHY", "GLYCINE ENCEPHALOPATHY; GCE", "GCE", "Hyperglycinemia nonketotic", "NKA", "Hyperglycinemia, Nonketotic"]}
-{"question": "Gene Attenuated familial adenomatous polyposis has a genetic association with diseases such as", "references": ["NTHL1", "NTH1", "OCTS3", "hNTH1", "FAP3", "nth-like DNA glycosylase 1", "nth like DNA glycosylase 1"]}
-{"question": "Gene NSDHL has a genetic association with diseases such as", "references": ["CHILD syndrome", "Congenital hemidysplasia with ichthyosiform nevus and limbs defects", "CONGENITAL HEMIDYSPLASIA WITH ICHTHYOSIFORM ERYTHRODERMA AND LIMB DEFECTS", "Congenital Hemidysplasia with Ichthyosiform nevus and Limb Defects", "Ichthyosis, CHILD syndrome", "CHILD nevus", "Child Syndrome", "Ichthyosiform Erythroderma, Unilateral, With Ipsilateral Malformations, Especially Absence Deformity of Limbs"]}
-{"question": "Gene MED30 has a genetic association with diseases such as", "references": ["Kawasaki disease", "Kawasaki's disease", "MLNS", "acute febrile MCLS", "acute febrile mucocutaneous lymph node syndrome [MCLS]", "mucocutaneous lymph node syndrome", "Kawasaki disease, KD", "acute febrile mucocutaneous lymph node syndrome", "Infantile Polyarteritis Nodosa", "KAWASAKI DISEASE", "Kd", "Infantile Polyarteritis"]}
-{"question": "Gene PCBD2 has a genetic association with diseases such as", "references": ["type 2 diabetes", "NIDDM", "non-insulin-dependent diabetes mellitus", "type II diabetes mellitus", "Diabetes mellitus type 2", "Rare insulin-independent diabetes mellitus", "Diabetes Mellitus, Type 2", "type 2 diabetes mellitus", "diabetes (type 2)"]}
-{"question": "Gene MLPH has a genetic association with diseases such as", "references": ["prostate cancer", "malignant tumor of the prostate", "prostatic cancer", "tumor of the prostate", "malignant neoplasm of the prostate", "prostate cancer, familial", "hereditary prostate cancer"]}
-{"question": "Gene Dolichol kinase deficiency has a genetic association with diseases such as", "references": ["DOLK", "CDG1M", "DK", "DK1", "SEC59", "TMEM15", "dolichol kinase"]}
-{"question": "Gene Ichthyosis prematurity syndrome has a genetic association with diseases such as", "references": ["SLC27A4", "ACSVL4", "FATP4", "IPS", "solute carrier family 27 member 4"]}
-{"question": "Gene HIVEP1 has a genetic association with diseases such as", "references": ["non-controlled substance abuse", "abuse of licit drugs", "abuse of licit drug", "noncontrolled substance use disorder", "non-controlled substance use disorder", "abuse of noncontrolled substances", "noncontrolled substance related disorder", "non-controlled substance related disorder", "legal substance abuse", "licit drug use disorder", "non-controlled medication abuse", "toxicomania", "toxic substance abuse", "substance dependence", "drug addiction"]}
-{"question": "Gene Nakajo syndrome has a genetic association with diseases such as", "references": ["PSMB8", "ALDD", "D6S216", "D6S216E", "JMP", "LMP7", "NKJO", "PSMB5i", "RING10", "proteasome subunit beta 8", "PRAAS1", "proteasome 20S subunit beta 8"]}
-{"question": "Gene BMPER has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene Morquio syndrome has a genetic association with diseases such as", "references": ["GALNS", "galactosamine (N-acetyl)-6-sulfatase", "GALNAC6S", "GAS", "GalN6S", "MPS4A", "GLB1", "EBP", "ELNR1", "MPS4B", "galactosidase beta 1"]}
-{"question": "Gene Ichthyosis with confetti has a genetic association with diseases such as", "references": ["KRT10", "BCIE", "BIE", "CK10", "EHK", "K10", "KPP", "keratin 10"]}
-{"question": "Gene MRAS has a genetic association with diseases such as", "references": ["amyotrophic lateral sclerosis", "ALS", "Lou Gehrig's disease", "motor neuron disease, bulbar", "Lou Gehrig disease", "Charcot disease", "Amyotrophic lateral sclerosis", "motor neurone disease", "Lou Gehrig's disease", "coronary artery disease", "CAD", "atherosclerotic heart disease", "coronary heart disease", "ischemic heart disease", "IHD", "atherosclerotic cardiovascular disease", "CHD (coronary heart disease)", "coronary arteriosclerosis", "CHD", "coronary artery arteriosclerosis (disease)", "atherosclerosis of coronary artery", "Coronary Atherosclerosis"]}
-{"question": "Gene congenital dyserythropoietic anemia has a genetic association with diseases such as", "references": ["KLF1", "CDAN4", "EKLF", "HBFQTL6", "INLU", "Kruppel-like factor 1 (erythroid)", "Kruppel like factor 1", "EKLF/KLF1"]}
-{"question": "Gene NACC1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene TBX22 has a genetic association with diseases such as", "references": ["Abruzzo\u2013Erickson syndrome", "Cleft palate-coloboma-deafness syndrome", "ABRUZZO-ERICKSON SYNDROME; ABERS", "Charge-Like Syndrome, X-Linked", "ABERS", "CHARGE-like syndrome", "CHARGE like syndrome X-linked", "ABRUZZO-ERICKSON SYNDROME", "Abruzzo-Erickson syndrome"]}
-{"question": "Gene SH3BP4 has a genetic association with diseases such as", "references": ["cleft lip and cleft palate", "cleft palate", "cleft lip", "cheilopalatoschisis", "Complete unilateral cleft palate with cleft lip (disorder)", "Unilateral complete cleft palate with cleft lip", "Unilateral complete cleft palate with cleft lip (disorder)", "Unilateral incomplete cleft palate with cleft lip", "Unilateral incomplete cleft palate with cleft lip (disorder)", "cleft palate with cleft lip, unilateral, complete", "cleft palate with cleft lip, unilateral, incomplete", "incomplete unilateral cleft palate with cleft lip (disorder)", "orofacial cleft", "obsolete cheilopalatoschisis"]}
-{"question": "Gene PAPA syndrome has a genetic association with diseases such as", "references": ["PSTPIP1", "CD2BP1", "CD2BP1L", "CD2BP1S", "H-PIP", "PAPAS", "PSTPIP", "proline-serine-threonine phosphatase interacting protein 1"]}
-{"question": "Gene HOXD13 has a genetic association with diseases such as", "references": ["VACTERL association", "VACTERL/VATER association", "vater ASSOCIATION", "vater association (disorder)", "vater association [dup] (disorder)", "VATER syndrome", "VACTERL association", "Vertebral Abnormalities, Anal Atresia, Cardiac Abnormalities, Tracheo-Esophageal Fistula, Renal Anomalies, Limb Defects Syndrome", "VATER/VACTERL ASSOCIATION"]}
-{"question": "Gene XDH has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene bronchiectasis has a genetic association with diseases such as", "references": ["SCNN1B", "BESC1", "ENaCb", "ENaCbeta", "SCNEB", "sodium channel epithelial 1 beta subunit", "LIDLS1", "sodium channel epithelial 1 subunit beta", "SCNN1A", "BESC2", "ENaCa", "ENaCalpha", "SCNEA", "SCNN1", "sodium channel epithelial 1 alpha subunit", "LIDLS3", "sodium channel epithelial 1 subunit alpha", "SCNN1G", "BESC3", "ENaCg", "ENaCgamma", "PHA1", "SCNEG", "sodium channel epithelial 1 gamma subunit", "LDLS2", "sodium channel epithelial 1 subunit gamma"]}
-{"question": "Gene GPR35 has a genetic association with diseases such as", "references": ["inflammatory bowel diseases", "IBD", "inflammatory bowel disease", "ulcerative colitis", "hemorrhagic colitis", "Ulcerative Colitis", "Colitis Ulcerative", "Ulcerative colitis", "left-sided ulcerative colitis", "UC"]}
-{"question": "Gene Thiel-Behnke corneal dystrophy has a genetic association with diseases such as", "references": ["TGFBI", "BIGH3", "CDB1", "CDG2", "CDGG1", "CSD", "CSD1", "CSD2", "CSD3", "EBMD", "LCD1", "transforming growth factor beta induced"]}
-{"question": "Gene MLLT10 has a genetic association with diseases such as", "references": ["meningioma", "intracranial meningioma", "meningothelial cell tumor", "neoplasm of the meninges", "primary Meningeal tumor", "supratentorial meningioma", "meningioma by site", "Meningeal Tumor", "Tumor of Meninges", "Tumor of the Meninges", "neoplasm of meningeal cluster", "Meninges Tumor", "tumor of meningeal cluster", "meningeal cluster neoplasm (disease)", "meningeal cluster tumor", "meningeal cluster rare nervous system tumor"]}
-{"question": "Gene GABBR2 has a genetic association with diseases such as", "references": ["post-traumatic stress disorder", "PTSD", "traumatic neurosis", "posttraumatic stress disorder", "Stress Disorders, Post-Traumatic", "post traumatic stress disorder"]}
-{"question": "Gene VTCN1 has a genetic association with diseases such as", "references": ["juvenile rheumatoid arthritis", "acute juvenile rheumatoid arthritis", "juvenile chronic polyarthritis", "monarticular juvenile rheumatoid arthritis", "pauciarticular juvenile arthritis", "systemic juvenile rheumatoid arthritis", "juvenile idiopathic arthritis", "chronic childhood arthritis"]}
-{"question": "Gene OPTN has a genetic association with diseases such as", "references": ["mammary Paget's disease", "Paget cell neoplasm", "Paget's disease", "Paget's disease of the breast", "mammary Paget disease", "paget disease", "Paget Disease", "Paget Cell Neoplasm", "Paget's Cell Neoplasm", "Paget's Disease", "Paget's Disease, Mammary"]}
-{"question": "Gene RASAL2 has a genetic association with diseases such as", "references": ["smallpox", "ordinary smallpox", "variola", "variola vera"]}
-{"question": "Gene NRAS has a genetic association with diseases such as", "references": ["juvenile myelomonocytic leukemia", "Juvenile Chronic Myeloid Leukemia", "Juvenile Myelomonocytic Leukemia", "Juvenile chronic myelomonocytic leukemia", "Chronic Myelomonocytic Leukemia", "JUVENILE MYELOMONOCYTIC LEUKEMIA; JMML", "Juvenile Chronic Myelogenous Leukemia", "JCML", "Leukemia, Chronic Myelomonocytic", "Leukemia, Juvenile Myelomonocytic", "JMML", "RAS-associated autoimmune leukoproliferative disorder", "RAS-associated autoimmune leukoproliferative disease", "Autoimmune lymphoproliferative syndrome type 4", "autoimmune lymphoproliferative syndrome type 4", "ALPS type 4", "ALPS type IV", "ALPS4", "RALD", "autoimmune lymphoproliferative syndrome type IV", "RAS-associated autoimmune leukoproliferative disorder", "RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER; RALD", "Autoimmune Lymphoproliferative Syndrome, Type 4", "Neurocutaneous melanosis", "Neuromelanosis", "Neurocutaneous melanosis", "MELANOSIS, NEUROCUTANEOUS; NCMS", "NCMS", "MELANOSIS, NEUROCUTANEOUS", "NCM", "follicular thyroid cancer", "follicular thyroid carcinoma", "Follicular adenocarcinoma (morphologic abnormality)", "Follicular adenocarcinoma, well differentiated (morphologic abnormality)", "Follicular carcinoma", "Follicular carcinoma of the Thyroid gland", "Follicular thyroid carcinoma (disorder)", "thyroid adenocarcinoma", "thyroid gland follicular carcinoma", "Follicular adenocarcinoma", "Follicular adenocarcinoma, well differentiated", "THYROID CANCER, NONMEDULLARY, 2; NMTC2", "THYROID CANCER, NONMEDULLARY, 2", "Thyroid Cancer, Nonmedullary, type 2", "NMTC2", "Adenocarcinoma, Follicular"]}
-{"question": "Gene renal agenesis has a genetic association with diseases such as", "references": ["ITGA8", "integrin subunit alpha 8"]}
-{"question": "Gene beta thalassemia has a genetic association with diseases such as", "references": ["BCL11A", "BCL11A-L", "BCL11A-S", "BCL11A-XL", "BCL11a-M", "CTIP1", "EVI9", "HBFQTL5", "ZNF856", "B-cell CLL/lymphoma 11A", "DILOS", "B cell CLL/lymphoma 11A", "BCL11A, BAF complex component", "BAF chromatin remodeling complex subunit BCL11A", "SMARCM1"]}
-{"question": "Gene hypertrophic cardiomyopathy has a genetic association with diseases such as", "references": ["ESRRG", "ERR3", "ERRgamma", "NR3B3", "estrogen related receptor gamma", "ERRg", "ERR-gamma", "FGF1", "AFGF", "ECGF", "ECGF-beta", "ECGFA", "ECGFB", "FGF-1", "FGF-alpha", "FGFA", "GLIO703", "HBGF-1", "HBGF1", "fibroblast growth factor 1", "CAV3", "LGMD1C", "LQT9", "VIP-21", "VIP21", "caveolin 3", "MPDT", "RMD2"]}
-{"question": "Gene Thyroid dyshormonogenesis has a genetic association with diseases such as", "references": ["IYD", "iodotyrosine deiodinase", "C6orf71", "DEHAL1", "TDH4", "dJ422F24.1", "IYD-1", "DUOX2", "LNOX2", "NOXEF2", "P138-TOX", "TDH6", "THOX2", "dual oxidase 2"]}
-{"question": "Gene CTSK has a genetic association with diseases such as", "references": ["pycnodysostosis", "Pyknodysostosis", "Pycd", "PYCNODYSOSTOSIS", "PKND"]}
-{"question": "Gene KCNIP4 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene congenital disorder of glycosylation Iq has a genetic association with diseases such as", "references": ["SRD5A3", "CDG1P", "CDG1Q", "KRIZI", "SRD5A2L", "SRD5A2L1", "steroid 5 alpha-reductase 3"]}
-{"question": "Gene CACNA1C has a genetic association with diseases such as", "references": ["schizophrenia", "Morel-Kraepelin disease", "Kraepelin-Morel disease", "dementia pr\u00e6cox", "dementia praecox", "schizophrenia-1", "bipolar disorder", "BP", "manic depression", "BPAD", "major depressive disorder", "recurrent depressive disorder", "major depression", "unipolar depression", "MDD", "clinical depression", "recurrent major depression", "single major depressive episode", "recurrent major depression in complete remission", "recurrent major depressive episodes, in full remission (disorder)", "major depression disorder", "depression", "Timothy syndrome", "long QT syndrome 8", "LQT8", "Long QT syndrome-syndactyly syndrome", "TIMOTHY SYNDROME; TS", "TIMOTHY SYNDROME", "TS", "Long QT syndrome type 8", "Long Qt Syndrome With Syndactyly", "obsolete Timothy syndrome"]}
-{"question": "Gene citrullinemia has a genetic association with diseases such as", "references": ["ASS1", "ASS", "CTLN1", "Argininosuccinate synthetase 1", "argininosuccinate synthase 1"]}
-{"question": "Gene Camisa disease has a genetic association with diseases such as", "references": ["LORICRIN", "loricrin", "LOR", "loricrin cornified envelope precursor protein"]}
-{"question": "Gene Alveolar capillary dysplasia has a genetic association with diseases such as", "references": ["FOXF1", "ACDMPV", "FKHL5", "FREAC1", "forkhead box F1"]}
-{"question": "Gene CPT1A has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "lipid metabolism disorder", "fatty acid metabolism disorder", "dyslipidemia", "lipid metabolism disorders", "carnitine palmitoyltransferase I deficiency", "CPT I deficiency", "carnitine palmitoyl transferase 1A deficiency", "hepatic CPT deficiency type I", "L-CPT1 deficiency", "carnitine palmitoyl transferase IA deficiency", "hepatic carnitine palmitoyl transferase I deficiency", "CPT1A deficiency", "hepatic carnitine palmitoyl transferase 1 deficiency", "Cpt Deficiency, Hepatic, Type 1", "Carnitine palmitoyltransferase 1A deficiency", "Cpt 1 Deficiency", "L-CPTI deficiency", "Hepatic carnitine palmitoyltransferase 1 deficiency", "Carnitine palmitoyl transferase 1 deficiency", "CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY", "Hepatic CPT1", "L-CPT 1 deficiency"]}
-{"question": "Gene SLC39A11 has a genetic association with diseases such as", "references": ["amyotrophic lateral sclerosis", "ALS", "Lou Gehrig's disease", "motor neuron disease, bulbar", "Lou Gehrig disease", "Charcot disease", "Amyotrophic lateral sclerosis", "motor neurone disease", "Lou Gehrig's disease"]}
-{"question": "Gene IGF2 has a genetic association with diseases such as", "references": ["Silver-Russell syndrome", "Silver Russell Dwarfism", "Russell-Silver Dwarfism", "Silver-Russell Dwarfism", "Russell-Silver Syndrome", "SILVER-RUSSELL SYNDROME; SRS", "SRS", "SILVER-RUSSELL SYNDROME", "Silver\u2013Russell dwarfism"]}
-{"question": "Gene HLA-DQA1 has a genetic association with diseases such as", "references": ["asthma", "exercise-induced asthma", "chronic obstructive asthma", "chronic obstructive asthma with status asthmaticus", "chronic obstructive asthma with acute exacerbation", "bronchial hyperreactivity", "Exercise induced asthma", "Asthma", "asthma brionchiole", "membranous glomerulonephritis", "Membranous Glomerulonephritis", "Membranous glomerulonephritis (disorder)", "Membranous nephropathy NOS", "membranous nephropathy", "lupus nephritis class 5", "Membranous Glomerulonephropathy", "chronic lymphocytic leukemia", "B-cell chronic lymphocytic leukemia", "CLL", "chronic lymphatic leukemia", "lymphoplasmacytic leukemia", "B-cell chronic lymphoid leukemia", "B-Cell Chronic Lymphogenous Leukemia", "Chronic Lymphocytic Leukemia (CLL)", "Hematopoeitic - Chronic Lymphocytic Leukemia (CLL)", "Chronic B-Cell Lymphocytic Leukemia", "B-Cell CLL", "Leukemia, Chronic Lymphatic", "B Cell CLL", "Small lymphocytic lymphoma", "BCLL", "LEUKEMIA, CHRONIC LYMPHOCYTIC; CLL", "B Cell Chronic Lymphocytic Leukemia", "B-CLL", "Chronic Lymphocytic Leukemia", "B Cell Lymphocytic Leukemia", "Chronic Lymphogenous Leukemia", "B-Cell Lymphocytic Leukemia", "LEUKEMIA, CHRONIC LYMPHOCYTIC", "Chronic lymphocytic leukemia, NOS", "Chronic lymphocytic leukemia; CLL", "Leukemia, Lymphocytic, Chronic, B-Cell", "Chronic lymphocytic leukaemia", "chronic lymphocytic leukaemia", "systemic lupus erythematosus", "SLE", "lupus", "Lupus Erythematosus, systemic", "SLE - Lupus Erythematosus, systemic", "disseminated lupus erythematosus", "Systemic lupus erythematosus", "coeliac disease", "celiac sprue", "celiac disease", "nontropical sprue", "endemic sprue", "gluten enteropathy", "idiopathic steatorrhea", "CeD"]}
-{"question": "Gene SUCLG2 has a genetic association with diseases such as", "references": ["astigmatism"]}
-{"question": "Gene membranoproliferative glomerulonephritis has a genetic association with diseases such as", "references": ["CFH", "AHUS1", "AMBP1", "ARMD4", "ARMS1", "CFHL3", "FH", "FHL1", "HF", "HF1", "HF2", "HUS", "complement factor H"]}
-{"question": "Gene Liebenberg syndrome has a genetic association with diseases such as", "references": ["PITX1", "BFT", "CCF", "LBNBG", "POTX", "PTX1", "paired like homeodomain 1"]}
-{"question": "Gene Hyperproinsulinemia has a genetic association with diseases such as", "references": ["INS", "IDDM", "IDDM1", "IDDM2", "ILPR", "IRDN", "MODY10", "insulin", "PNDM4", "\u30a4\u30f3\u30b7\u30e5\u30ea\u30f3"]}
-{"question": "Gene Kufs disease has a genetic association with diseases such as", "references": ["CLN6", "CLN4A", "HsT18960", "nclf", "ceroid-lipofuscinosis, neuronal 6, late infantile, variant", "CLN6, transmembrane ER protein", "CLN6 transmembrane ER protein", "CLN6A"]}
-{"question": "Gene CAMK2A has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene Kindler syndrome has a genetic association with diseases such as", "references": ["FERMT1", "C20orf42", "DTGCU2", "KIND1", "UNC112A", "URP1", "fermitin family member 1", "FERM domain containing kindlin 1"]}
-{"question": "Gene erythrokeratodermia variabilis has a genetic association with diseases such as", "references": ["GJB4", "CX30.3", "EKV", "gap junction protein beta 4", "EKVP2"]}
-{"question": "Gene rheumatoid arthritis has a genetic association with diseases such as", "references": ["SPRED2", "Spred-2", "sprouty related EVH1 domain containing 2", "CDK5RAP2", "C48", "Cep215", "MCPH3", "CDK5 regulatory subunit associated protein 2", "KIF5A", "D12S1889", "MY050", "NKHC", "SPG10", "kinesin family member 5A", "NEIMY", "ALS25", "ARID5B", "DESRT", "MRF-2", "MRF2", "AT-rich interaction domain 5B", "ATG5", "APG5", "APG5-LIKE", "APG5L", "ASP", "hAPG5", "autophagy related 5", "SCAR25", "CD226", "DNAM-1", "DNAM1", "PTA1", "TLiSA1", "CD226 molecule", "CDK6", "MCPH12", "PLSTIRE", "cyclin-dependent kinase 6", "cyclin dependent kinase 6", "EOMES", "TBR2", "Eomesodermin", "GATA3", "HDR", "HDRS", "GATA binding protein 3", "IL2RB", "CD122", "IL15RB", "P70-75", "interleukin 2 receptor subunit beta", "IMD63", "IL6R", "CD126", "IL-6R-1", "IL-6RA", "IL6Q", "IL6RA", "IL6RQ", "gp80", "Interleukin-6 receptor", "interleukin 6 receptor", "JAZF1", "TIP27", "ZNF802", "JAZF zinc finger 1", "NFKBIE", "IKBE", "NFKB inhibitor epsilon", "PADI4", "PAD", "PAD4", "PADI5", "PDI4", "PDI5", "peptidyl arginine deiminase 4", "PPIL4", "HDCME13P", "peptidylprolyl isomerase like 4", "PRKCH", "PKC-L", "PKCL", "PRKCL", "nPKC-eta", "protein kinase C eta", "PTPN2", "PTN2", "PTPT", "TC-PTP", "TCELLPTP", "TCPTP", "protein tyrosine phosphatase, non-receptor type 2", "protein tyrosine phosphatase non-receptor type 2", "RAD51B", "R51H2", "RAD51L1", "REC2", "RAD51 paralog B", "RASGRP1", "CALDAG-GEFI", "CALDAG-GEFII", "RASGRP", "hRasGRP1", "RAS guanyl releasing protein 1", "IMD64", "REL", "C-Rel", "REL proto-oncogene, NF-kB subunit", "HIVEN86A", "SFTPD", "COLEC7", "PSP-D", "SFTP4", "SP-D", "surfactant protein D", "STAT4", "SLEB11", "signal transducer and activator of transcription 4", "SYNGR1", "synaptogyrin 1", "TEC", "PSCTK4", "tec protein tyrosine kinase", "TYK2", "IMD35", "JTK1", "tyrosine kinase 2", "Non-receptor tyrosine-protein kinase", "UBASH3A", "CLIP4", "STS-2", "TULA", "TULA-1", "ubiquitin associated and SH3 domain containing A", "ARL15", "ARFRP2", "ADP ribosylation factor like GTPase 15", "RTKN2", "PLEKHK1", "bA531F24.1", "rhotekin 2", "ALPL", "AP-TNAP", "APTNAP", "HOPS", "TNAP", "TNSALP", "alkaline phosphatase, liver/bone/kidney", "TNALP", "alkaline phosphatase, biomineralization associated", "HPPA", "HPPI", "HPPC", "HPPO", "TNS-ALP", "SPSB1", "SSB-1", "SSB1", "splA/ryanodine receptor domain and SOCS box containing 1", "ENOX1", "CNOX", "PIG38", "bA64J21.1", "cCNOX", "ecto-NOX disulfide-thiol exchanger 1", "MDGA2", "MAMDC1", "c14_5286", "MAM domain containing glycosylphosphatidylinositol anchor 2", "PSMA4", "HC9", "HsT17706", "PSC9", "proteasome subunit alpha 4", "proteasome 20S subunit alpha 4", "RCHY1", "ARNIP", "CHIMP", "PIRH2", "PRO1996", "RNF199", "ZCHY", "ZNF363", "ring finger and CHY zinc finger domain containing 1", "ETFA", "EMA", "GA2", "MADD", "electron transfer flavoprotein alpha subunit", "electron transfer flavoprotein subunit alpha", "ANXA3", "ANX3", "annexin A3", "MICA", "MIC-A", "PERB11.1", "MHC class I polypeptide-related sequence A", "MHC class I chain\u2013related protein A", "MHC class I polypeptide\u2013related protein A", "BLK", "MODY11", "BLK proto-oncogene, Src family tyrosine kinase", "TRHDE", "PAP-II", "PGPEP2", "TRH-DE", "thyrotropin releasing hormone degrading enzyme", "ARHGEF3", "GEF3", "STA3", "XPLN", "Rho guanine nucleotide exchange factor 3", "CD247", "CD3-ZETA", "CD3H", "CD3Q", "CD3Z", "IMD25", "T3Z", "TCRZ", "CD247 molecule", "CD3zeta", "ELMO1", "CED-12", "CED12", "ELMO-1", "engulfment and cell motility 1", "IFI16", "IFNGIP1", "PYHIN2", "interferon gamma inducible protein 16", "IRF5", "SLEB10", "interferon regulatory factor 5", "SH2B3", "IDDM20", "LNK", "SH2B adaptor protein 3"]}
-{"question": "Gene glycine encephalopathy has a genetic association with diseases such as", "references": ["AMT", "aminomethyltransferase", "GCE", "GCST", "GCVT", "NKH", "GCSH", "GCE", "NKH", "glycine cleavage system protein H", "GLDC", "GCE", "GCSP", "HYGN1", "Glycine dehydrogenase", "glycine decarboxylase"]}
-{"question": "Gene PLAGL1 has a genetic association with diseases such as", "references": ["transient neonatal diabetes mellitus", "Tndm", "Tndm1", "Dmtn", "DIABETES MELLITUS, TRANSIENT NEONATAL, 1", "Diabetes Mellitus, Transient Neonatal, type 1"]}
-{"question": "Gene Autosomal recessive multiple epiphyseal dysplasia has a genetic association with diseases such as", "references": ["SLC26A2", "D5S1708", "DTD", "DTDST", "EDM4", "MST153", "MSTP157", "solute carrier family 26 member 2"]}
-{"question": "Gene Lathosterolosis has a genetic association with diseases such as", "references": ["SC5D", "ERG3", "S5DES", "SC5DL", "Sterol-C5-desaturase-like", "sterol-C5-desaturase"]}
-{"question": "Gene iridogoniodysgenesis syndrome has a genetic association with diseases such as", "references": ["PITX2", "ARP1", "Brx1", "IDG2", "IGDS", "IGDS2", "IHG2", "IRID2", "Otlx2", "PTX2", "RGS", "RIEG", "RIEG1", "RS", "paired like homeodomain 2", "ASGD4", "FOXC1", "ARA", "FKHL7", "FREAC-3", "FREAC3", "IGDA", "IHG1", "IRID1", "RIEG3", "forkhead box C1", "ASGD3"]}
-{"question": "Gene MYO1B has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene CBLB has a genetic association with diseases such as", "references": ["multiple sclerosis", "MS", "encephalomyelitis disseminata", "insular sclerosis", "disseminated sclerosis", "generalized multiple sclerosis", "Generalized multiple sclerosis (disorder)", "generalised multiple sclerosis", "Multiple sclerosis; MS", "Multiple sclerosis"]}
-{"question": "Gene CACNA2D3 has a genetic association with diseases such as", "references": ["endometrial cancer", "endometrial Ca", "malignant endometrial neoplasm", "malignant neoplasm of endometrium", "neoplasm of endometrium (disorder)", "primary malignant neoplasm of endometrium", "tumor of Endometrium", "Endometrial Tumor", "endometrium tumor", "endometrium neoplasm (disease)", "Tumor of the Endometrium", "smallpox", "ordinary smallpox", "variola", "variola vera"]}
-{"question": "Gene DNAH9 has a genetic association with diseases such as", "references": ["myopia", "near-sightedness", "short-sightedness", "near vision"]}
-{"question": "Gene KAT2B has a genetic association with diseases such as", "references": ["post-traumatic stress disorder", "PTSD", "traumatic neurosis", "posttraumatic stress disorder", "Stress Disorders, Post-Traumatic", "post traumatic stress disorder"]}
-{"question": "Gene SLC9A6 has a genetic association with diseases such as", "references": ["Christianson syndrome", "MRXSCH", "X-linked Angelman-like syndrome", "X-linked intellectual disability, South African type", "X-linked intellectual disability-craniofacial dysmorphism-epilepsy-ophthalmoplegia-cerebellar atrophy syndrome", "mental retardation, X-linked syndromic, Christianson type", "mental retardation, microcephaly, epilepsy, and ataxia syndrome", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHRISTIANSON TYPE; MRXSCH", "Intellectual disability x-linked syndromic Christianson type", "Angelman-Like Syndrome, X-Linked", "MRXS Christianson", "Intellectual disability microcephaly epilepsy and ataxia syndrome", "Angelman-like syndrome x-linked", "X-linked intellectual disability - craniofacial dysmorphism - epilepsy - ophthalmoplegia - cerebellar atrophy"]}
-{"question": "Gene ABCC12 has a genetic association with diseases such as", "references": ["amyotrophic lateral sclerosis", "ALS", "Lou Gehrig's disease", "motor neuron disease, bulbar", "Lou Gehrig disease", "Charcot disease", "Amyotrophic lateral sclerosis", "motor neurone disease", "Lou Gehrig's disease"]}
-{"question": "Gene IRX4 has a genetic association with diseases such as", "references": ["cardiovascular disease", "CV disease", "cardiovascular system disease", "myocardiovascular system disease", "heart, respiratory, and blood vessel disease", "diseases of the circulatory system", "cardiovascular diseases", "disease of subdivision of hemolymphoid system", "CVD"]}
-{"question": "Gene CLN6 has a genetic association with diseases such as", "references": ["neuronal ceroid lipofuscinosis", "hereditary ceroid lipofuscinosis", "neuronal ceroid lipofuscinosis (disorder)", "NCL"]}
-{"question": "Gene creatine transporter deficiency has a genetic association with diseases such as", "references": ["SLC6A8", "CCDS1", "CRT", "CRTR", "CT1", "CTR5", "solute carrier family 6 member 8"]}
-{"question": "Gene acrodysostosis has a genetic association with diseases such as", "references": ["PDE4D", "ACRDYS2", "DPDE3", "HSPDE4D", "PDE43", "PDE4DN2", "STRK1", "phosphodiesterase 4D", "PRKAR1A", "ACRDYS1", "ADOHR", "CAR", "CNC", "CNC1", "PKR1", "PPNAD1", "PRKAR1", "TSE1", "protein kinase cAMP-dependent type I regulatory subunit alpha"]}
-{"question": "Gene cerebrotendinous xanthomatosis has a genetic association with diseases such as", "references": ["CYP27A1", "CP27", "CTX", "CYP27", "cytochrome P450 family 27 subfamily A member 1"]}
-{"question": "Gene leprosy has a genetic association with diseases such as", "references": ["RPS6KA4", "MSK2", "RSK-B", "S6K-alpha-4", "ribosomal protein S6 kinase A4", "RIPK2", "CARD3", "CARDIAK", "CCK", "GIG30", "RICK", "RIP2", "receptor interacting serine/threonine kinase 2", "TNFSF15", "TL1", "TL1A", "VEGI", "VEGI192A", "Vascular endothelial growth inhibitor", "TNLG1B", "tumor necrosis factor superfamily member 15", "TNF superfamily member 15"]}
-{"question": "Gene SRGAP1 has a genetic association with diseases such as", "references": ["follicular thyroid cancer", "follicular thyroid carcinoma", "Follicular adenocarcinoma (morphologic abnormality)", "Follicular adenocarcinoma, well differentiated (morphologic abnormality)", "Follicular carcinoma", "Follicular carcinoma of the Thyroid gland", "Follicular thyroid carcinoma (disorder)", "thyroid adenocarcinoma", "thyroid gland follicular carcinoma", "Follicular adenocarcinoma", "Follicular adenocarcinoma, well differentiated", "THYROID CANCER, NONMEDULLARY, 2; NMTC2", "THYROID CANCER, NONMEDULLARY, 2", "Thyroid Cancer, Nonmedullary, type 2", "NMTC2", "Adenocarcinoma, Follicular"]}
-{"question": "Gene Michelin tire baby syndrome has a genetic association with diseases such as", "references": ["TUBB", "CDCBM6", "M40", "OK/SW-cl.56", "TUBB1", "TUBB5", "CSCSC1", "tubulin beta class I", "MAPRE2", "EB1", "EB2", "RP1", "CSCSC2", "microtubule associated protein RP/EB family member 2"]}
-{"question": "Gene focal facial dermal dysplasia has a genetic association with diseases such as", "references": ["TWIST2", "DERMO1", "FFDD3", "SETLSS", "bHLHa39", "AMS", "BBRSAY", "twist family bHLH transcription factor 2"]}
-{"question": "Gene Hailey-Hailey disease has a genetic association with diseases such as", "references": ["ATP2C1", "ATP2C1A", "BCPM", "HHD", "PMR1", "SPCA1", "hSPCA1", "ATPase secretory pathway Ca2+ transporting 1"]}
-{"question": "Gene blepharophimosis, ptosis, and epicanthus inversus syndrome has a genetic association with diseases such as", "references": ["FOXL2", "BPES", "BPES1", "PFRK", "PINTO", "POF3", "forkhead box L2"]}
-{"question": "Gene osteoporosis has a genetic association with diseases such as", "references": ["MECOM", "AML1-EVI-1", "EVI1", "MDS1", "MDS1-EVI1", "PRDM3", "RUSAT2", "MDS1 and EVI1 complex locus", "KMT8E", "ALDH7A1", "ATQ1", "EPD", "PDE", "aldehyde dehydrogenase 7 family member A1", "SOX6", "HSSOX6", "SOXD", "SRY-box 6", "SRY-box transcription factor 6", "TOLCAS", "WNT1", "BMND16", "INT1", "OI15", "Wnt family member 1", "LGR4", "BNMD17", "GPR48", "leucine-rich repeat containing G protein-coupled receptor 4", "leucine rich repeat containing G protein-coupled receptor 4", "DPSL", "LRP5", "BMND1", "EVR1", "EVR4", "HBM", "LR3", "LRP-5", "LRP7", "OPPG", "OPS", "OPTA1", "VBCH2", "LDL receptor related protein 5", "PCLD4", "LRP-7", "PLS3", "BMND18", "T-plastin", "plastin 3"]}
-{"question": "Gene nasopharynx carcinoma has a genetic association with diseases such as", "references": ["TNFRSF19", "TAJ", "TAJ-alpha", "TRADE", "TROY", "tumor necrosis factor receptor superfamily member 19", "TNF receptor superfamily member 19", "ITGA9", "ALPHA-RLC", "ITGA4L", "RLC", "integrin subunit alpha 9"]}
-{"question": "Gene CSF1R has a genetic association with diseases such as", "references": ["Hereditary diffuse leukoencephalopathy with spheroids", "Familial dementia, Neumann type", "LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS", "Gliosis, Familial Progressive Subcortical", "Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia", "LEUKOENCEPHALOPATHY, DIFFUSE HEREDITARY, WITH SPHEROIDS; HDLS", "Subcortical gliosis of Neumann", "Leukoencephalopathy With Neuroaxonal Spheroids, Autosomal Dominant", "GPSC", "Dementia, Familial, Neumann Type", "ALSP", "POLD", "Pigmentary orthochromatic leukodystrophy", "Familial progressive subcortical gliosis", "FPSG", "HDLS", "Autosomal dominant leukoencephalopathy with neuroaxonal spheroids", "Hereditary diffuse leukoencephalopathy", "Hereditary diffuse leukoencephalopathy with spheroid"]}
-{"question": "Gene Barraquer\u2013Simons syndrome has a genetic association with diseases such as", "references": ["LMNB2", "lamin B2", "LAMB2", "LMN2", "EPM9", "MCPH27"]}
-{"question": "Gene SLC16A2 has a genetic association with diseases such as", "references": ["Allan-Herndon-Dudley syndrome", "ALLAN-HERNDON SYNDROME", "ALLAN-HERNDON-DUDLEY SYNDROME", "T3 Resistance", "X-linked intellectual disability-hypotonia syndrome", "Monocarboxylate transporter 8 deficiency", "AHDS", "MCT8 deficiency", "ALLAN-HERNDON-DUDLEY SYNDROME; AHDS", "MCT8-Specific Thyroid Hormone Cell Membrane Transporter Deficiency", "Mental Retardation, X-Linked, With Hypotonia", "Monocarboxylate transporter-8 deficiency", "Triiodothyronine resistence", "X-linked intellectual disability with hypotonia", "Triiodothyronine Resistance", "Mental Retardation and Muscular Atrophy", "T3 resisitence", "Intellectual disability and muscular atrophy"]}
-{"question": "Gene PMP22 has a genetic association with diseases such as", "references": ["hereditary neuropathy with liability to pressure palsies", "HNPP", "current pressure-sensitive neuropathy", "familial recurrent polyneuropathy", "heterozygous microdeletion 17p11.2p12", "potato-grubbing palsy", "tomaculous neuropathy", "tulip-bulb digger's palsy", "NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES", "NEUROPATHY, HEREDITARY, WITH LIABILITY TO PRESSURE PALSIES; HNPP", "Polyneuropathy, Familial Recurrent", "neuropathy, recurrent, with pressure palsies", "chronic inflammatory demyelinating polyradiculoneuropathy", "CIDP", "chronic inflammatory demyelinating polyradiculoneuropathy (disorder)", "chronic inflammatory demyelinating polyneuritis", "chronic relapsing polyneuropathy", "chronic inflammatory demyelinating polyneuropathy", "Polyneuropathy, Inflammatory Demyelinating, Acute", "Chronic inflammatory demyelinating polyneuropathy", "Chronic inflammatory demyelinating polyradiculoneuropathy", "Polyneuropathy, Inflammatory Demyelinating, Chronic", "Charcot\u2013Marie\u2013Tooth disease", "Charcot-Marie-Tooth disease", "CMT - Charcot-Marie-Tooth disease", "Charcot Marie Tooth muscular atrophy", "Peroneal muscular atrophy", "Charcot-Marie-Tooth disease\u3001C-M-T"]}
-{"question": "Gene Leber hereditary optic neuropathy has a genetic association with diseases such as", "references": ["ATP6", "ATPase6", "MTATP6", "ATP synthase F0 subunit 6", "ND4", "MTND4", "MT-ND4", "NADH dehydrogenase, subunit 4 (complex I)", "NADH dehydrogenase subunit 4", "ND2", "complex I ND2 subunit", "NAD2", "NADH-ubiquinone oxidoreductase chain 2", "MT-ND2", "MTND2", "NADH dehydrogenase subunit 2", "ND4L", "MTND4L", "MT-ND4L", "NADH dehydrogenase, subunit 4L (complex I)", "NADH dehydrogenase subunit 4L", "CYTB", "MTCYB", "MT-CYB", "cytochrome b", "ND6", "MTND6", "MT-ND6", "NADH dehydrogenase, subunit 6 (complex I)", "NADH dehydrogenase subunit 6", "ND5", "mitochondrially encoded NADH dehydrogenase 5", "MTND5", "NADH dehydrogenase, subunit 5 (complex I)", "NADH dehydrogenase subunit 5", "ND1", "MTND1", "MT-ND1", "NADH dehydrogenase, subunit 1 (complex I)", "NADH dehydrogenase subunit 1", "COX3", "COIII", "MTCO3", "Cytochrome c oxidase subunit III", "cytochrome c oxidase III", "COX1", "mitochondrially encoded cytochrome c oxidase I", "COI", "MTCO1", "Main subunit of cytochrome c oxidase", "CO I", "cytochrome c oxidase subunit I"]}
-{"question": "Gene ulnar-mammary syndrome has a genetic association with diseases such as", "references": ["TBX3", "TBX3-ISO", "UMS", "XHL", "T-box 3", "T-box transcription factor 3"]}
-{"question": "Gene TP63 has a genetic association with diseases such as", "references": ["adenocarcinoma of the lung", "lung adenocarcinoma", "nonsmall cell adenocarcinoma", "adenocarcinoma of lung", "bronchogenic lung adenocarcinoma", "Adenocarcinoma of the Lung", "non-small cell lung adenocarcinoma", "pulmonary adenocarcinoma", "lung cancer", "malignant lung tumor", "malignant neoplasm of lung", "ADULT syndrome", "acro-dermato-ungual-lacrimal-tooth syndrome", "Acrodermatounguallacrimaltooth syndrome", "Pigment anomaly-ectrodactyly-hypodontia syndrome", "ADULT syndrome", "Propping-Zerres syndrome", "Limb\u2013mammary syndrome", "LIMB-MAMMARY SYNDROME", "LIMB-MAMMARY SYNDROME; LMS", "LMS"]}
-{"question": "Gene seborrheic keratosis has a genetic association with diseases such as", "references": ["PIK3CA", "CLOVE", "CWS5", "MCAP", "MCM", "MCMTC", "PI3K", "p110-alpha", "PI3K-alpha", "phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha", "CLAPO", "CCM4", "FGFR3", "ACH", "CD333", "CEK2", "HSFGFR3EX", "JTK4", "fibroblast growth factor receptor 3"]}
-{"question": "Gene DPP6 has a genetic association with diseases such as", "references": ["colorectal cancer", "colon cancer", "rectal cancer", "large intestine cancer", "Colorectal cancer, familial", "bowel cancer", "colon and rectal cancer", "post-traumatic stress disorder", "PTSD", "traumatic neurosis", "posttraumatic stress disorder", "Stress Disorders, Post-Traumatic", "post traumatic stress disorder", "pancreatic cancer", "Ca tail of pancreas", "Ca head of pancreas", "Ca body of pancreas", "malignant neoplasm of head of pancreas", "malignant neoplasm of tail of pancreas", "malignant neoplasm of body of pancreas", "amyotrophic lateral sclerosis", "ALS", "Lou Gehrig's disease", "motor neuron disease, bulbar", "Lou Gehrig disease", "Charcot disease", "Amyotrophic lateral sclerosis", "motor neurone disease", "Lou Gehrig's disease"]}
-{"question": "Gene medulloblastoma has a genetic association with diseases such as", "references": ["SUFU", "PRO1280", "SUFUH", "SUFUXL", "SUFU negative regulator of hedgehog signaling", "JBTS32"]}
-{"question": "Gene PYGL has a genetic association with diseases such as", "references": ["glycogen storage disease VI", "Hers' disease", "Glycogen storage disease, type VI (disorder)", "glycogen storage disease type VI", "hepatic glycogen phosphorylase deficiency (disorder)", "hepatophosphorylase deficiency glycogenosis", "hepatic glycogen phosphorylase deficiency", "Glycogen storage disease type 6", "Hers Disease", "Glycogen storage disease due to liver glycogen phosphorylase deficiency", "Glycogenosis type VI", "GLYCOGEN STORAGE DISEASE VI; GSD6", "Glycogenosis due to liver glycogen phosphorylase deficiency", "GSD due to liver glycogen phosphorylase deficiency", "Hepatic phosphorylase deficiency", "GSD type VI", "Gsd 6", "Liver glycogen phosphorylase deficiency", "Phosphorylase Deficiency Glycogen-Storage Disease of Liver", "GSD6", "GSD type 6", "GLYCOGEN STORAGE DISEASE VI", "Glycogenosis type 6"]}
-{"question": "Gene SNAI2 has a genetic association with diseases such as", "references": ["Waardenburg syndrome type 2D", "Waardenburg syndrome type IID", "WS2D", "Waardenburg Syndrome, Type 2D", "WAARDENBURG SYNDROME, TYPE 2D; WS2D", "Waardenburg Syndrome Type 2D", "piebaldism", "PIEBALD TRAIT", "Partial albinism (disorder)", "Partial albinism", "PBT", "PIEBALD TRAIT; PBT", "Piebaldism"]}
-{"question": "Gene hepatocellular carcinoma has a genetic association with diseases such as", "references": ["STAT4", "SLEB11", "signal transducer and activator of transcription 4", "GRIK1", "EAA3", "EEA3", "GLR5", "GLUR5", "GluK1", "gluR-5", "glutamate ionotropic receptor kainate type subunit 1", "C2", "ARMD14", "CO2", "complement component 2", "complement C2"]}
-{"question": "Gene head and neck squamous cell carcinoma has a genetic association with diseases such as", "references": ["ING3", "Eaf4", "ING2", "MEAF4", "p47ING3", "inhibitor of growth family member 3", "ING1", "p24ING1c", "p33", "p33ING1", "p33ING1b", "p47", "p47ING1a", "inhibitor of growth family member 1", "TNFRSF10B", "CD262", "DR5", "KILLER", "KILLER/DR5", "TRAIL-R2", "TRAILR2", "TRICK2", "TRICK2A", "TRICK2B", "TRICKB", "ZTNFR9", "tumor necrosis factor receptor superfamily member 10b", "TNF receptor superfamily member 10b"]}
-{"question": "Gene DSG3 has a genetic association with diseases such as", "references": ["Parkinson's disease", "paralysis agitans", "parkinsonismus idiopathicus", "Parkinson", "Parkinson disease"]}
-{"question": "Gene Mal de Meleda has a genetic association with diseases such as", "references": ["SLURP1", "ANUP", "ARS", "ArsB", "LY6LS", "MDM", "secreted LY6/PLAUR domain containing 1", "LY6-MT"]}
-{"question": "Gene MKKS has a genetic association with diseases such as", "references": ["McKusick\u2013Kaufman syndrome", "Hydrometrocolpos, Postaxial Polydactyly, and Congenital Heart Malformation", "Kaufman-Mckusick Syndrome", "Kaufman McKusick syndrome", "MCKUSICK-KAUFMAN SYNDROME", "Hydrometrocolpos-postaxial polydactyly syndrome", "MKKS", "HMCS", "McKusick Kaufman syndrome", "Hydrometrocolpos Syndrome", "MCKUSICK-KAUFMAN SYNDROME; MKKS", "McKusick-Kaufman syndrome", "hydrometrocolpos-postaxial polydactyly syndrome", "hydrometrocolpos syndrome", "hydrometrocolpos, postaxial polydactyly, and congenital heart malformation"]}
-{"question": "Gene FREM1 has a genetic association with diseases such as", "references": ["trigonocephaly", "Trigonocephaly type 2", "Craniosynostosis, Metopic", "Trigonocephaly 2", "Trigono 2", "Trigono2", "trigonocephalus", "trigonocephalia"]}
-{"question": "Gene MAP2K5 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene FUCA1 has a genetic association with diseases such as", "references": ["fucosidosis", "Alpha-L-Fucosidase deficiency", "A-fucosidase deficiency", "Fucosidosis (disorder)", "alpha fucosidase deficiency", "Lysosomal storage disease caused by defective alpha-L-fucosidase with accumulation of fucose in the tissues", "FUCOSIDOSIS"]}
-{"question": "Gene COG5 has a genetic association with diseases such as", "references": ["osteoarthritis", "degenerative arthritis", "degenerative joint disease", "hypertrophic arthritis", "osteoarthrosis", "osteoarthrosis and allied disorder"]}
-{"question": "Gene ZNF320 has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene Keratosis follicularis spinulosa decalvans has a genetic association with diseases such as", "references": ["MBTPS2", "BRESEK", "IFAP", "KFSD", "KFSDX", "OLMSX", "S2P", "membrane bound transcription factor peptidase, site 2", "OI19"]}
-{"question": "Gene GNA12 has a genetic association with diseases such as", "references": ["ulcerative colitis", "hemorrhagic colitis", "Ulcerative Colitis", "Colitis Ulcerative", "Ulcerative colitis", "left-sided ulcerative colitis", "UC"]}
-{"question": "Gene paroxysmal nocturnal hemoglobinuria has a genetic association with diseases such as", "references": ["PIGT", "MCAHS3", "NDAP", "PNH2", "CGI-06", "phosphatidylinositol glycan anchor biosynthesis class T"]}
-{"question": "Gene EEM syndrome has a genetic association with diseases such as", "references": ["CDH3", "CDHP", "HJMD", "PCAD", "cadherin 3"]}
-{"question": "Gene congenital disorder of glycosylation has a genetic association with diseases such as", "references": ["PMM2", "CDG1", "CDG1a", "CDGS", "PMI", "PMI1", "PMM 2", "phosphomannomutase 2"]}
-{"question": "Gene NGLY1-deficiency has a genetic association with diseases such as", "references": ["NGLY1", "CDG1V", "PNG1", "PNGase", "CDDG", "N-glycanase 1", "PNG-1"]}
-{"question": "Gene IRF6 has a genetic association with diseases such as", "references": ["cleft lip and cleft palate", "cleft palate", "cleft lip", "cheilopalatoschisis", "Complete unilateral cleft palate with cleft lip (disorder)", "Unilateral complete cleft palate with cleft lip", "Unilateral complete cleft palate with cleft lip (disorder)", "Unilateral incomplete cleft palate with cleft lip", "Unilateral incomplete cleft palate with cleft lip (disorder)", "cleft palate with cleft lip, unilateral, complete", "cleft palate with cleft lip, unilateral, incomplete", "incomplete unilateral cleft palate with cleft lip (disorder)", "orofacial cleft", "obsolete cheilopalatoschisis", "Van der Woude syndrome", "lip-pit syndrome", "VAN DER WOUDE SYNDROME 1; VWS1", "VWS1", "Vdws", "Van Der Woude Syndrome type 1", "Cleft 51P And/Or Palate With Mucous Cysts of Lower 51P", "VAN DER WOUDE SYNDROME 1", "popliteal pterygium syndrome", "facio-genito-popliteal syndrome", "popliteal web syndrome", "POPLITEAL PTERYGIUM SYNDROME; PPS", "POPLITEAL PTERYGIUM SYNDROME", "Faciogenitopopliteal Syndrome", "Cleft Lip/Palate, Paramedian Mucous Cysts of the Lower Lip, Popliteal Pterygium, Digital and Genital Anomalies", "popliteal pterygium syndrome, autosomal dominant", "PPS"]}
-{"question": "Gene RFC5 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene BICD1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "pulmonary emphysema", "emphysema", "pancreatic cancer", "Ca tail of pancreas", "Ca head of pancreas", "Ca body of pancreas", "malignant neoplasm of head of pancreas", "malignant neoplasm of tail of pancreas", "malignant neoplasm of body of pancreas"]}
-{"question": "Gene CTBP2 has a genetic association with diseases such as", "references": ["prostate cancer", "malignant tumor of the prostate", "prostatic cancer", "tumor of the prostate", "malignant neoplasm of the prostate", "prostate cancer, familial", "hereditary prostate cancer"]}
-{"question": "Gene PRKCH has a genetic association with diseases such as", "references": ["rheumatoid arthritis", "Arthritis or polyarthritis, rheumatic", "atrophic Arthritis", "Rheumatoid arthritis with vasculitis", "Malignant rheumatoid arthritis", "Rheumatoid arthritis"]}
-{"question": "Gene BARD1 has a genetic association with diseases such as", "references": ["neuroblastoma", "NB", "neuroblastoma (Schwannian Stroma-Poor)"]}
-{"question": "Gene Familial cold urticaria has a genetic association with diseases such as", "references": ["NLRP3", "AGTAVPRL", "AII", "AVP", "C1orf7", "CIAS1", "CLR1.1", "FCAS", "FCAS1", "FCU", "MWS", "NALP3", "PYPAF1", "NLR family, pyrin domain containing 3", "NLR family pyrin domain containing 3", "DFNA34", "KEFH"]}
-{"question": "Gene MMP17 has a genetic association with diseases such as", "references": ["migraine", "migraine variant", "sick headache", "migraine with or without aura", "migraine disorders", "migraine disorder"]}
-{"question": "Gene ESR1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "breast cancer", "malignant neoplasm of breast", "malignant tumor of the breast", "mammary cancer", "primary breast cancer", "breast disorder", "alcohol dependence", "alcoholism", "alcohol dependence syndrome", "alcohol addiction"]}
-{"question": "Gene PAX6 has a genetic association with diseases such as", "references": ["Morning glory disc anomaly", "coloboma of optic nerve", "Coloboma of optic disc (disorder)", "Coloboma of optic disc", "Optic Nerve Head Pits, Bilateral Congenital", "Morning Glory Disc Anomaly", "Morning glory syndrome"]}
-{"question": "Gene Pashayan syndrome has a genetic association with diseases such as", "references": ["DCHS1", "CDH19", "CDH25", "CDHR6", "FIB1", "PCDH16", "VMLDS1", "MVP2", "dachsous cadherin-related 1"]}
-{"question": "Gene ITGA8 has a genetic association with diseases such as", "references": ["periodontitis", "pyorrhea", "chronic pericementitis", "periodontium inflammation", "periodontiumitis", "Parkinson's disease", "paralysis agitans", "parkinsonismus idiopathicus", "Parkinson", "Parkinson disease"]}
-{"question": "Gene Emberger syndrome has a genetic association with diseases such as", "references": ["GATA2", "DCML", "IMD21", "MONOMAC", "NFE1B", "GATA binding protein 2"]}
-{"question": "Gene Ectopia lentis has a genetic association with diseases such as", "references": ["ADAMTSL4", "ADAMTSL-4", "ECTOL2", "TSRC1", "ADAMTS like 4"]}
-{"question": "Gene MGP has a genetic association with diseases such as", "references": ["Keutel syndrome", "KEUTEL SYNDROME; KTLS", "KEUTEL SYNDROME", "Pulmonic stenosis-brachytelephalangism-calcification of cartilages syndrome", "Pulmonic stenosis brachytelephalangism and calcification of cartilages", "Pulmonic Stenosis, Brachytelephalangism, and Calcification of Cartilages", "KTLS"]}
-{"question": "Gene NLRP3 has a genetic association with diseases such as", "references": ["Muckle-Wells syndrome", "Uda Syndrome", "Cryopyrin-Associated Periodic Syndrome 2", "MUCKLE-WELLS SYNDROME; MWS", "MWS", "Urticaria-Deafness-Amyloidosis Syndrome", "MUCKLE-WELLS SYNDROME", "Neutrophilic urticaria", "CINCA syndrome", "NOMID syndrome", "chronic infantile neurological cutaneous articular syndrome", "Prieur-Griscelli syndrome", "infantile-onset multisystem inflammatory disease", "cryopyrin-associated periodic syndrome 3", "IOMID syndrome", "chronic neurologic cutaneous and articular syndrome", "neonatal-onset multisystem inflammatory disease", "chronic infantile neurological cutaneous and articular syndrome", "CINCA/NOMID", "CINCA", "CINCA SYNDROME", "CINCA SYNDROME; CINCA", "Multisystem Inflammatory Disease, Neonatal-Onset", "NOMID"]}
-{"question": "Gene ZMIZ1 has a genetic association with diseases such as", "references": ["type 2 diabetes", "NIDDM", "non-insulin-dependent diabetes mellitus", "type II diabetes mellitus", "Diabetes mellitus type 2", "Rare insulin-independent diabetes mellitus", "Diabetes Mellitus, Type 2", "type 2 diabetes mellitus", "diabetes (type 2)", "breast cancer", "malignant neoplasm of breast", "malignant tumor of the breast", "mammary cancer", "primary breast cancer", "breast disorder", "psoriasis", "Crohn's disease", "regional enteritis", "Crohn disease", "Crohn's disease of colon (disorder)", "Crohn's disease of large bowel", "Granulomatous Colitis", "regional Ileitis", "regional colitis", "regional enteritis of small intestine with large intestine", "regional enteritis of the large bowel", "regional ileocolitis", "Crohn's disease of colon", "Crohn", "multiple sclerosis", "MS", "encephalomyelitis disseminata", "insular sclerosis", "disseminated sclerosis", "generalized multiple sclerosis", "Generalized multiple sclerosis (disorder)", "generalised multiple sclerosis", "Multiple sclerosis; MS", "Multiple sclerosis", "vitiligo", "el morenito ojos claros", "coeliac disease", "celiac sprue", "celiac disease", "nontropical sprue", "endemic sprue", "gluten enteropathy", "idiopathic steatorrhea", "CeD", "inflammatory bowel diseases", "IBD", "inflammatory bowel disease"]}
-{"question": "Gene Epstein\u2013Barr virus infection has a genetic association with diseases such as", "references": ["IRF8", "H-ICSBP", "ICSBP", "ICSBP1", "IMD32A", "IMD32B", "IRF-8", "interferon regulatory factor 8"]}
-{"question": "Gene SLITRK1 has a genetic association with diseases such as", "references": ["trichotillomania", "TTM", "trichotillosis", "hair pulling disorder"]}
-{"question": "Gene FTL has a genetic association with diseases such as", "references": ["Adult-onset basal ganglia disease", "neuroferritinopathy", "NBIA3", "Hereditary ferritinopathy", "Neuroferritinopathy; Basal Ganglia Disease, Adult-Onset", "Neuroferritinopathy", "Ferritin-related neurodegeneration", "Adult basal ganglia disease", "Neurodegeneration With Brain Iron Accumulation type 3", "NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3", "Basal Ganglia Disease, Adult-Onset", "NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 3; NBIA3"]}
-{"question": "Gene Reynolds syndrome has a genetic association with diseases such as", "references": ["LBR", "DHCR14B", "LMN2R", "PHA", "TDRD18", "lamin B receptor", "PHASK", "C14SR"]}
-{"question": "Gene GIPC3 has a genetic association with diseases such as", "references": ["nonsyndromic deafness", "nonsyndromic hearing loss", "nonsyndromic hereditary hearing loss", "Familial deafness", "Non-syndromic genetic deafness", "Isolated genetic deafness"]}
-{"question": "Gene CDON has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene SNAP29 has a genetic association with diseases such as", "references": ["CEDNIK syndrome", "cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome", "Cerebral dysgenesis-neuropathy-ichthyosis-palmoplantar keratoderma syndrome", "CEREBRAL DYSGENESIS, NEUROPATHY, ICHTHYOSIS, AND PALMOPLANTAR KERATODERMA SYNDROME"]}
-{"question": "Gene PROCR has a genetic association with diseases such as", "references": ["amyotrophic lateral sclerosis", "ALS", "Lou Gehrig's disease", "motor neuron disease, bulbar", "Lou Gehrig disease", "Charcot disease", "Amyotrophic lateral sclerosis", "motor neurone disease", "Lou Gehrig's disease"]}
-{"question": "Gene KDM4B has a genetic association with diseases such as", "references": ["periodontitis", "pyorrhea", "chronic pericementitis", "periodontium inflammation", "periodontiumitis"]}
-{"question": "Gene ovarian hyperstimulation syndrome has a genetic association with diseases such as", "references": ["FSHR", "FSHR1", "FSHRO", "LGR1", "ODG1", "follicle stimulating hormone receptor"]}
-{"question": "Gene PPM1F has a genetic association with diseases such as", "references": ["attention deficit hyperactivity disorder", "ADHD", "hyperkinetic disorder", "attention deficit disorder", "AD/HD", "A.D.H.D", "attention deficit/hyperactivity disorder", "attention deficit hyperactivity syndrome", "Attention Deficit Disorder with Hyperactivity", "ADDH"]}
-{"question": "Gene GPC6 has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease", "obesity", "corpulence", "overfatness", "fatness", "obese", "attention deficit hyperactivity disorder", "ADHD", "hyperkinetic disorder", "attention deficit disorder", "AD/HD", "A.D.H.D", "attention deficit/hyperactivity disorder", "attention deficit hyperactivity syndrome", "Attention Deficit Disorder with Hyperactivity", "ADDH"]}
-{"question": "Gene ATG16L1 has a genetic association with diseases such as", "references": ["Crohn's disease", "regional enteritis", "Crohn disease", "Crohn's disease of colon (disorder)", "Crohn's disease of large bowel", "Granulomatous Colitis", "regional Ileitis", "regional colitis", "regional enteritis of small intestine with large intestine", "regional enteritis of the large bowel", "regional ileocolitis", "Crohn's disease of colon", "Crohn"]}
-{"question": "Gene KRT12 has a genetic association with diseases such as", "references": ["Meesmann corneal dystrophy", "MECD", "Stocker-Holt dystrophy", "juvenile hereditary epithelial dystrophy", "CORNEAL DYSTROPHY, MEESMANN; MECD", "Corneal Dystrophy, Juvenile Epithelial, of Meesmann", "Meesmann corneal epithelial dystrophy", "Corneal Dystrophy, Meesmann Epithelial", "Juvenile Epithelial of Meesmann Corneal Dystrophy", "Meesmann Corneal Dystrophy", "Corneal dystrophy, juvenile epithelial of Meesmann", "CORNEAL DYSTROPHY, MEESMANN", "Meesman dystrophy", "Juvenile hereditary epithelial dystrophy of Meesmann"]}
-{"question": "Gene mulibrey nanism has a genetic association with diseases such as", "references": ["TRIM37", "MUL", "POB1", "TEF3", "tripartite motif containing 37"]}
-{"question": "Gene SETD2 has a genetic association with diseases such as", "references": ["acute myeloid leukemia", "AML - acute Myeloid Leukemia", "Leukemia, Myelocytic, acute", "acute myeloblastic leukemia", "acute myelogenous leukemia", "Acute myelogenous leukemia; AML", "Acute Granulocytic Leukemia", "LEUKEMIA, ACUTE MYELOID; AML", "Acute non lymphoblastic leukemia", "myeloid leukemia, acute", "LEUKEMIA, ACUTE MYELOID", "ANLL", "Hematopoeitic - Acute Myleogenous Leukemia (AML)", "Acute Myeloid Leukemia", "Leukemia, Acute Myeloid, Susceptibility to", "Acute Myeloid Leukemia (AML)", "Leukemia, Acute Myelogenous", "Acute Myelogenous Leukemias", "AML", "Acute Nonlymphocytic Leukemia", "Acute Myelocytic Leukemia", "acute myeloid leukaemia"]}
-{"question": "Gene TBX4 has a genetic association with diseases such as", "references": ["Ischiopatellar dysplasia", "coxopodopatellar syndrome", "Scott-Taor syndrome", "SPS", "Ischiopatellar dysplasia", "SMALL PATELLA SYNDROME", "SMALL PATELLA SYNDROME; SPS", "ischiocoxopodopatellar syndrome", "ICPPS"]}
-{"question": "Gene glycogen storage disease IV has a genetic association with diseases such as", "references": ["GBE1", "APBD", "GBE", "GSD4", "glucan (1,4-alpha-), branching enzyme 1", "1,4-alpha-glucan branching enzyme 1"]}
-{"question": "Gene AUTS2 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "bipolar disorder", "BP", "manic depression", "BPAD", "alcohol abuse", "ethanol abuse", "harmful use of alcohol", "alcohol use disorder"]}
-{"question": "Gene Carpenter syndrome has a genetic association with diseases such as", "references": ["RAB23", "HSPC137", "RAB23, member RAS oncogene family", "MEGF8", "C19orf49", "CRPT2", "EGFL4", "SBP1", "Multiple Epidermal Growth Factor-like Domains 8", "multiple EGF like domains 8"]}
-{"question": "Gene retinopathy of prematurity has a genetic association with diseases such as", "references": ["FZD4", "CD344", "EVR1", "FEVR", "FZD4S", "Fz-4", "Fz4", "FzE4", "GPCR", "hFz4", "frizzled class receptor 4"]}
-{"question": "Gene dyschromatosis universalis hereditaria has a genetic association with diseases such as", "references": ["ABCB6", "ABC", "ABC14", "DUH3", "LAN", "MCOPCB7", "MTABC3", "PRP", "umat", "PSHK2", "ATP binding cassette subfamily B member 6 (Langereis blood group)"]}
-{"question": "Gene HAPLN1 has a genetic association with diseases such as", "references": ["prostate cancer", "malignant tumor of the prostate", "prostatic cancer", "tumor of the prostate", "malignant neoplasm of the prostate", "prostate cancer, familial", "hereditary prostate cancer"]}
-{"question": "Gene EPB41 has a genetic association with diseases such as", "references": ["amyotrophic lateral sclerosis", "ALS", "Lou Gehrig's disease", "motor neuron disease, bulbar", "Lou Gehrig disease", "Charcot disease", "Amyotrophic lateral sclerosis", "motor neurone disease", "Lou Gehrig's disease"]}
-{"question": "Gene chronic obstructive pulmonary disease has a genetic association with diseases such as", "references": ["CHRNA3", "LNCR2", "NACHRA3", "PAOD2", "cholinergic receptor nicotinic alpha 3 subunit", "BAIPRCK", "FAM13A", "ARHGAP48", "FAM13A1", "Family with sequence similarity 13, member A1", "family with sequence similarity 13 member A", "TGFB2", "LDS4", "TGF-beta2", "transforming growth factor beta 2", "G-TSF", "SCGB1A1", "CC10", "CC16", "CCPBP", "CCSP", "UGB", "UP-1", "UP1", "secretoglobin family 1A member 1", "ASRGL1", "ALP", "ALP1", "CRASH", "asparaginase like 1", "asparaginase and isoaspartyl peptidase 1", "ANXA11", "ANX11", "CAP50", "annexin A11", "CAP-50", "ALS23", "HLA-C", "D6S204", "HLA-JY3", "HLC-C", "PSORS1", "HLAC", "major histocompatibility complex, class I, C", "MHC", "SFTPD", "COLEC7", "PSP-D", "SFTP4", "SP-D", "surfactant protein D", "JAKMIP3", "C10orf14", "C10orf39", "Jamip3", "NECC2", "bA140A10.5", "Janus kinase and microtubule interacting protein 3", "P2RX7", "P2X7", "purinergic receptor P2X 7", "EYA1", "BOP", "BOR", "BOS1", "OFC1", "EYA transcriptional coactivator and phosphatase 1", "ANXA5", "ANX5", "ENX2", "HEL-S-7", "PP4", "RPRGL3", "annexin A5", "CPB-I", "VAC-alph", "PLCE1", "NPHS3", "PLCE", "PPLC", "phospholipase C epsilon 1", "FTO", "ALKBH9", "GDFD", "BMIQ14", "fat mass and obesity associated", "FTO, alpha-ketoglutarate dependent dioxygenase"]}
-{"question": "Gene catecholaminergic polymorphic ventricular tachycardia has a genetic association with diseases such as", "references": ["RYR2", "ARVC2", "ARVD2", "RYR-2", "RyR", "VTSIP", "ryanodine receptor 2", "VACRDS"]}
-{"question": "Gene endometriosis has a genetic association with diseases such as", "references": ["PDE1C", "Hcam3", "cam-PDE 1C", "hCam-3", "phosphodiesterase 1C", "DFNA74", "IL33", "C9orf26", "DVS27", "IL1F11", "NF-HEV", "NFEHEV", "Interleukin 33", "IL-33", "IL-1F11", "VEZT", "VEZATIN", "vezatin, adherens junctions transmembrane protein", "KSR2", "kinase suppressor of ras 2", "GREB1", "growth regulation by estrogen in breast cancer 1", "growth regulating estrogen receptor binding 1"]}
-{"question": "Gene ITPKC has a genetic association with diseases such as", "references": ["Kawasaki disease", "Kawasaki's disease", "MLNS", "acute febrile MCLS", "acute febrile mucocutaneous lymph node syndrome [MCLS]", "mucocutaneous lymph node syndrome", "Kawasaki disease, KD", "acute febrile mucocutaneous lymph node syndrome", "Infantile Polyarteritis Nodosa", "KAWASAKI DISEASE", "Kd", "Infantile Polyarteritis"]}
-{"question": "Gene PHACTR1 has a genetic association with diseases such as", "references": ["coronary artery disease", "CAD", "atherosclerotic heart disease", "coronary heart disease", "ischemic heart disease", "IHD", "atherosclerotic cardiovascular disease", "CHD (coronary heart disease)", "coronary arteriosclerosis", "CHD", "coronary artery arteriosclerosis (disease)", "atherosclerosis of coronary artery", "Coronary Atherosclerosis", "migraine", "migraine variant", "sick headache", "migraine with or without aura", "migraine disorders", "migraine disorder", "myocardial infarction", "MI", "infarctus myocardii acutus", "heart attack", "myocardial infarct"]}
-{"question": "Gene Muir-Torre syndrome has a genetic association with diseases such as", "references": ["MSH2", "mutS homolog 2", "COCA1", "FCC1", "HNPCC", "HNPCC1", "LCFS2", "hMSH2", "MMRCS2", "MLH1", "mutL homolog 1", "COCA2", "FCC2", "HNPCC", "HNPCC2", "hMLH1"]}
-{"question": "Gene Sturge\u2013Weber syndrome has a genetic association with diseases such as", "references": ["GNAQ", "CMC1", "G-ALPHA-q", "GAQ", "SWS", "G protein subunit alpha q"]}
-{"question": "Gene DOCK6 has a genetic association with diseases such as", "references": ["coronary artery disease", "CAD", "atherosclerotic heart disease", "coronary heart disease", "ischemic heart disease", "IHD", "atherosclerotic cardiovascular disease", "CHD (coronary heart disease)", "coronary arteriosclerosis", "CHD", "coronary artery arteriosclerosis (disease)", "atherosclerosis of coronary artery", "Coronary Atherosclerosis"]}
-{"question": "Gene SEMA5A has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "Parkinson's disease", "paralysis agitans", "parkinsonismus idiopathicus", "Parkinson", "Parkinson disease"]}
-{"question": "Gene OR5T3 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene sideroblastic anaemia P has a genetic association with diseases such as", "references": ["ALAS2", "ALAS-E", "ALASE", "ANH1", "ASB", "XLDPP", "XLEPP", "XLSA", "SIDBA1", "5'-aminolevulinate synthase 2"]}
-{"question": "Gene CPNE4 has a genetic association with diseases such as", "references": ["amyotrophic lateral sclerosis", "ALS", "Lou Gehrig's disease", "motor neuron disease, bulbar", "Lou Gehrig disease", "Charcot disease", "Amyotrophic lateral sclerosis", "motor neurone disease", "Lou Gehrig's disease"]}
-{"question": "Gene adermatoglyphia has a genetic association with diseases such as", "references": ["SMARCAD1", "ADERM", "ETL1", "HEL1", "SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1", "BASNS", "HRZ"]}
-{"question": "Gene ILF3 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene chronic granulomatous disease has a genetic association with diseases such as", "references": ["NCF2", "NCF-2", "NOXA2", "P67-PHOX", "P67PHOX", "Neutrophil cytosolic factor 2", "NCF4", "NCF", "P40PHOX", "SH3PXD4", "Neutrophil cytosolic factor 4", "CGD3", "CYBB", "AMCBX2", "CGD", "GP91-1", "GP91-PHOX", "GP91PHOX", "IMD34", "NOX2", "p91-PHOX", "cytochrome b-245 beta chain", "CGDX", "CYBA", "p22-PHOX", "Cytochrome b-245, alpha polypeptide", "cytochrome b-245 alpha chain", "CGD4"]}
-{"question": "Gene CNGB3 has a genetic association with diseases such as", "references": ["Stargardt disease", "STARGARDT DISEASE 1", "STARGARDT DISEASE 1; STGD1", "Early-onset severe retinal dystrophy", "Stargardt Disease type 1", "Fundus Flavimaculatus", "STGD1", "Macular Dystrophy With Flecks, Type 1", "Retinal Dystrophy, Early-Onset Severe", "Macular Degeneration, Juvenile", "Stgd", "EOSRD", "SECORD"]}
-{"question": "Gene TIMP3 has a genetic association with diseases such as", "references": ["Sorsby's fundus dystrophy", "hemorrhagic macular dystrophy", "SFD", "pseudoinflammatory fundus dystrophy of Sorsby", "SORSBY FUNDUS DYSTROPHY; SFD", "Fundus Dystrophy, Pseudoinflammatory, of Sorsby", "Macular Dystrophy, Hemorrhagic", "Sorsby pseudoinflammatory fundus dystrophy", "SORSBY FUNDUS DYSTROPHY"]}
-{"question": "Gene CTH has a genetic association with diseases such as", "references": ["cystathioninuria", "cystathione gamma-lyase deficiency syndrome", "gamma-cystathionase deficiency", "cystathionase deficiency", "CYSTATHIONINURIA"]}
-{"question": "Gene Progressive myoclonus epilepsy has a genetic association with diseases such as", "references": ["GOSR2", "Bos1", "EPM6", "GS27", "golgi SNAP receptor complex member 2", "KCTD7", "CLN14", "EPM3", "potassium channel tetramerization domain containing 7", "SCARB2", "AMRF", "CD36L2", "EPM4", "HLGP85", "LGP85", "LIMP-2", "LIMPII", "SR-BII", "scavenger receptor class B member 2", "PRICKLE1", "EPM1B", "RILP", "prickle planar cell polarity protein 1"]}
-{"question": "Gene chronic inflammatory demyelinating polyradiculoneuropathy has a genetic association with diseases such as", "references": ["PMP22", "CMT1A", "CMT1E", "DSS", "GAS-3", "HMSNIA", "HNPP", "Sujojp110", "GAS3", "peripheral myelin protein 22", "CIDP", "Sp110"]}
-{"question": "Gene Burkitt lymphoma has a genetic association with diseases such as", "references": ["MYC", "MRTL", "MYCC", "bHLHe39", "c-Myc", "v-myc avian myelocytomatosis viral oncogene homolog", "MYC proto-oncogene, bHLH transcription factor", "Genes, myc", "c-myc"]}
-{"question": "Gene NLGN1 has a genetic association with diseases such as", "references": ["periodontitis", "pyorrhea", "chronic pericementitis", "periodontium inflammation", "periodontiumitis"]}
-{"question": "Gene popliteal pterygium syndrome has a genetic association with diseases such as", "references": ["IRF6", "LPS", "OFC6", "PIT", "PPS", "PPS1", "VWS", "VWS1", "interferon regulatory factor 6", "RIPK4", "ANKK2", "ANKRD3", "DIK", "NKRD3", "PKK", "PPS2", "RIP4", "receptor interacting serine/threonine kinase 4", "CHANDS"]}
-{"question": "Gene KALRN has a genetic association with diseases such as", "references": ["schizophrenia", "Morel-Kraepelin disease", "Kraepelin-Morel disease", "dementia pr\u00e6cox", "dementia praecox", "schizophrenia-1"]}
-{"question": "Gene TRPV4 has a genetic association with diseases such as", "references": ["Parastremmatic dwarfism", "Parastremmatic dysplasia", "PARASTREMMATIC DWARFISM", "parastremmatic dwarfism", "neuromuscular disease"]}
-{"question": "Gene GPR141 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene STAT6 has a genetic association with diseases such as", "references": ["eosinophilic esophagitis", "EoE", "Eosinophilic esophagitis"]}
-{"question": "Gene RPS6KA3 has a genetic association with diseases such as", "references": ["Coffin-Lowry syndrome", "Coffin-Lowry syndrome (disorder)", "Coffin syndrome 1", "Lean spastic dwarfism", "Mental retardation with osteocartilaginous abnormalities", "Dwarfism, lean spastic type", "Coffin syndrome", "COFFIN-LOWRY SYNDROME", "COFFIN-LOWRY SYNDROME; CLS", "CLS"]}
-{"question": "Gene long QT syndrome has a genetic association with diseases such as", "references": ["KCNQ1", "ATFB1", "ATFB3", "JLNS1", "KCNA8", "KCNA9", "KVLQT1", "Kv1.9", "Kv7.1", "LQT", "LQT1", "RWS", "SQT2", "WRS", "potassium voltage-gated channel subfamily Q member 1", "CALM1", "CALML2", "CAMI", "CPVT4", "DD132", "PHKD", "caM", "LQT14", "Calmodulin 1", "calmodulin 1 (phosphorylase kinase, delta)", "CAMC", "CAMB", "CAMIII", "CAM3", "CAM2", "CALM2", "CAMII", "PHKD", "PHKD2", "LQT15", "caM", "calmodulin 2 (phosphorylase kinase, delta)", "calmodulin 2", "CAMC", "CAM1", "CAMIII", "CAM3", "CALM", "CALML2", "CALM3", "HEL-S-72", "PHKD", "PHKD3", "calmodulin 3 (phosphorylase kinase, delta)", "CaM", "CaMIII", "calmodulin 3", "CAM1", "CAMB", "CALM", "CAM2", "CPVT6", "LQT16"]}
-{"question": "Gene KBG syndrome has a genetic association with diseases such as", "references": ["ANKRD11", "ANCO-1", "ANCO1", "LZ16", "T13", "ankyrin repeat domain 11"]}
-{"question": "Gene RIT2 has a genetic association with diseases such as", "references": ["Parkinson's disease", "paralysis agitans", "parkinsonismus idiopathicus", "Parkinson", "Parkinson disease"]}
-{"question": "Gene ARHGAP18 has a genetic association with diseases such as", "references": ["vasculitis", "Angiitis", "Vasculitis Syndrome"]}
-{"question": "Gene ND6 has a genetic association with diseases such as", "references": ["Leber hereditary optic neuropathy", "LHON", "Leber optic atrophy", "Leber's optic atrophy", "Leber's optic atrophy (disorder)", "optic atrophy, Leber's", "Leber's hereditary optic neuropathy", "Laber'shereditary optic neuropathy", "Leber Hereditary Optic Neuropathy", "Optic Atrophy, Hereditary, Leber", "MELAS syndrome", "mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes", "MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES", "Mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes", "Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes", "MELAS", "Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke", "MITOCHONDRIAL MYOPATHY, ENCEPHALOPATHY, LACTIC ACIDOSIS, AND STROKE-LIKE EPISODES; MELAS", "Melas Syndrome"]}
-{"question": "Gene Down syndrome has a genetic association with diseases such as", "references": ["human chromosome 21", "chr21", "Homo sapiens chromosome 21", "21"]}
-{"question": "Gene systemic lupus erythematosus has a genetic association with diseases such as", "references": ["STAT4", "SLEB11", "signal transducer and activator of transcription 4", "TNPO3", "IPO12", "LGMD1F", "MTR10A", "TRN-SR", "TRN-SR2", "TRNSR", "transportin 3", "LGMDD2", "MTG1", "GTP", "GTPBP7", "mitochondrial ribosome associated GTPase 1", "GPR19", "G protein-coupled receptor 19", "BANK1", "BANK", "B-cell scaffold protein with ankyrin repeats 1", "B cell scaffold protein with ankyrin repeats 1", "TNFAIP3", "A20", "OTUD7C", "TNFA1P2", "AISBL", "TNF alpha induced protein 3", "TNIP1", "ABIN-1", "NAF1", "VAN", "nip40-1", "TNFAIP3 interacting protein 1", "UBE2L3", "E2-F1", "L-UBC", "UBCH7", "UbcM4", "ubiquitin conjugating enzyme E2 L3", "CLEC16A", "Gop-1", "KIAA0350", "C-type lectin domain family 16 member A", "C-type lectin domain containing 16A", "SLC15A4", "PHT1", "PTR4", "FP12591", "solute carrier family 15 member 4", "ELF1", "E74 like ETS transcription factor 1", "EFTUD1", "RIA1", "RASGRP3", "GRP3", "RAS guanyl releasing protein 3", "AFF1", "AF4", "MLLT2", "PBM1", "AF4/FMR2 family member 1", "LEF1", "LEF-1", "TCF10", "TCF1ALPHA", "TCF7L3", "lymphoid enhancer binding factor 1", "TNXB", "EDS3", "HXBL", "TENX", "TN-X", "TNX", "TNXB1", "TNXB2", "TNXBS", "VUR8", "XB", "XBS", "tenascin XB", "EDSCLL", "EDSCLL1", "LAMC2", "B2T", "BM600", "CSF", "EBR2", "EBR2A", "LAMB2T", "LAMNB2", "Laminin, gamma 2", "laminin subunit gamma 2", "OR4A15", "OR11-118", "olfactory receptor family 4 subfamily A member 15", "TMC2", "C20orf145", "dJ686C3.3", "transmembrane channel like 2", "ETS1", "ETS-1", "EWSR2", "p54", "c-ets-1", "ETS proto-oncogene 1, transcription factor", "BLK", "MODY11", "BLK proto-oncogene, Src family tyrosine kinase", "NTNG2", "LHLL9381", "Lmnt2", "NTNG1", "bA479K20.1", "netrin G2", "NEDBASH", "HLA-DQA1", "CD", "CELIAC1", "DQ-A1", "GSE", "HLA-DQA", "Major histocompatibility complex, class II, DQ alpha 1", "DQA1", "DNASE1L3", "DHP2", "DNAS1L3", "LSD", "SLEB16", "deoxyribonuclease I like 3", "deoxyribonuclease 1 like 3"]}
-{"question": "Gene Li-Fraumeni syndrome has a genetic association with diseases such as", "references": ["CHEK2", "CDS1", "CHK2", "HuCds1", "LFS2", "PP1425", "RAD53", "hCds1", "checkpoint kinase 2"]}
-{"question": "Gene PNMA8A has a genetic association with diseases such as", "references": ["colorectal cancer", "colon cancer", "rectal cancer", "large intestine cancer", "Colorectal cancer, familial", "bowel cancer", "colon and rectal cancer"]}
-{"question": "Gene CTDSPL has a genetic association with diseases such as", "references": ["prostate cancer", "malignant tumor of the prostate", "prostatic cancer", "tumor of the prostate", "malignant neoplasm of the prostate", "prostate cancer, familial", "hereditary prostate cancer"]}
-{"question": "Gene BRAF has a genetic association with diseases such as", "references": ["colorectal cancer", "colon cancer", "rectal cancer", "large intestine cancer", "Colorectal cancer, familial", "bowel cancer", "colon and rectal cancer", "non-Hodgkin lymphoma", "non-Hodgkin's lymphoma", "non-Hodgkin's", "Non-Hodgkin Lymphoma", "LYMPHOMA, NON-HODGKIN, FAMILIAL", "tumors of the hematopoietic and lymphoid tissues", "Non Hodgkins Lymphoma", "Non Hodgkin Lymphoma"]}
-{"question": "Gene oculopharyngeal muscular dystrophy has a genetic association with diseases such as", "references": ["PABPN1", "OPMD", "PAB2", "PABII", "PABP-2", "PABP2", "poly(A) binding protein nuclear 1"]}
-{"question": "Gene KLKB1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene S100P has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene meningioma has a genetic association with diseases such as", "references": ["MLLT10", "AF10", "myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10", "MLLT10, histone lysine methyltransferase DOT1L cofactor", "AKT1", "AKT", "CWS6", "PKB", "PKB-ALPHA", "PRKBA", "RAC", "RAC-ALPHA", "AKT serine/threonine kinase 1"]}
-{"question": "Gene HHIPL1 has a genetic association with diseases such as", "references": ["coronary artery disease", "CAD", "atherosclerotic heart disease", "coronary heart disease", "ischemic heart disease", "IHD", "atherosclerotic cardiovascular disease", "CHD (coronary heart disease)", "coronary arteriosclerosis", "CHD", "coronary artery arteriosclerosis (disease)", "atherosclerosis of coronary artery", "Coronary Atherosclerosis"]}
-{"question": "Gene Liddle syndrome has a genetic association with diseases such as", "references": ["SCNN1B", "BESC1", "ENaCb", "ENaCbeta", "SCNEB", "sodium channel epithelial 1 beta subunit", "LIDLS1", "sodium channel epithelial 1 subunit beta", "SCNN1G", "BESC3", "ENaCg", "ENaCgamma", "PHA1", "SCNEG", "sodium channel epithelial 1 gamma subunit", "LDLS2", "sodium channel epithelial 1 subunit gamma"]}
-{"question": "Gene DSCAM has a genetic association with diseases such as", "references": ["tuberculosis", "hydrothorax", "Tuberculosis", "In the clinic. Tuberculosis", "TB", "phthisis", "phthisis pulmonalis", "consumption", "phtisis"]}
-{"question": "Gene BLK has a genetic association with diseases such as", "references": ["smallpox", "ordinary smallpox", "variola", "variola vera", "rheumatoid arthritis", "Arthritis or polyarthritis, rheumatic", "atrophic Arthritis", "Rheumatoid arthritis with vasculitis", "Malignant rheumatoid arthritis", "Rheumatoid arthritis", "systemic lupus erythematosus", "SLE", "lupus", "Lupus Erythematosus, systemic", "SLE - Lupus Erythematosus, systemic", "disseminated lupus erythematosus", "Systemic lupus erythematosus"]}
-{"question": "Gene CDH8 has a genetic association with diseases such as", "references": ["non-small-cell lung carcinoma", "NSCLC", "non-small cell lung carcinoma", "Non-small cell lung cancer (disorder)", "Non-small cell lung cancer", "Non Small Cell Lung Cancer NOS", "Non-small cell lung cancer, NOS", "Non-Small Cell Cancer of the Lung", "NSCLC - Non-Small Cell Lung Cancer", "Non-Small Cell Carcinoma of Lung", "Non-Small Cell Carcinoma of the Lung", "Non-Small Cell Cancer of Lung", "Carcinoma, Non-Small-Cell Lung", "lung non-small cell carcinoma", "non-small cell lung cancer"]}
-{"question": "Gene peroxisomal acyl-CoA oxidase deficiency has a genetic association with diseases such as", "references": ["ACOX1", "ACOX", "PALMCOX", "SCOX", "acyl-CoA oxidase 1, palmitoyl", "acyl-CoA oxidase 1", "MITCH"]}
-{"question": "Gene SETBP1 has a genetic association with diseases such as", "references": ["Schinzel\u2013Giedion syndrome", "Schinzel-Giedion midface-retraction syndrome", "SGS", "SCHINZEL-GIEDION MIDFACE RETRACTION SYNDROME", "myelodysplastic syndrome", "preleukemia", "MDS", "Myelodysplastic syndrome, NOS", "Myelodysplastic Syndrome, Susceptibility to", "Dysmyelopoietic Syndrome", "Myelodysplasia", "MYELODYSPLASTIC SYNDROME", "myelodysplastic syndromes", "smoldering leukemia", "Oligoblastic Leukemia", "Myelodysplastic Neoplasm", "MYELODYSPLASTIC SYNDROME; MDS", "Hematopoeitic - Myelodysplastic Syndrome (MDS)", "Myelodysplastic Syndrome/Neoplasm", "acute myeloid leukemia", "AML - acute Myeloid Leukemia", "Leukemia, Myelocytic, acute", "acute myeloblastic leukemia", "acute myelogenous leukemia", "Acute myelogenous leukemia; AML", "Acute Granulocytic Leukemia", "LEUKEMIA, ACUTE MYELOID; AML", "Acute non lymphoblastic leukemia", "myeloid leukemia, acute", "LEUKEMIA, ACUTE MYELOID", "ANLL", "Hematopoeitic - Acute Myleogenous Leukemia (AML)", "Acute Myeloid Leukemia", "Leukemia, Acute Myeloid, Susceptibility to", "Acute Myeloid Leukemia (AML)", "Leukemia, Acute Myelogenous", "Acute Myelogenous Leukemias", "AML", "Acute Nonlymphocytic Leukemia", "Acute Myelocytic Leukemia", "acute myeloid leukaemia", "juvenile myelomonocytic leukemia", "Juvenile Chronic Myeloid Leukemia", "Juvenile Myelomonocytic Leukemia", "Juvenile chronic myelomonocytic leukemia", "Chronic Myelomonocytic Leukemia", "JUVENILE MYELOMONOCYTIC LEUKEMIA; JMML", "Juvenile Chronic Myelogenous Leukemia", "JCML", "Leukemia, Chronic Myelomonocytic", "Leukemia, Juvenile Myelomonocytic", "JMML"]}
-{"question": "Gene ZBTB17 has a genetic association with diseases such as", "references": ["dilated cardiomyopathy", "primary dilated cardiomyopathy", "Congestive cardiomyopathy", "Familial dilated cardiomyopathy", "Idiopathic dilation cardiomyopathy", "DCM"]}
-{"question": "Gene mood disorders has a genetic association with diseases such as", "references": ["PBRM1", "BAF180", "PB1", "polybromo 1", "SMARCH1", "RCC"]}
-{"question": "Gene hypochondroplasia has a genetic association with diseases such as", "references": ["FGFR3", "ACH", "CD333", "CEK2", "HSFGFR3EX", "JTK4", "fibroblast growth factor receptor 3"]}
-{"question": "Gene FBXL7 has a genetic association with diseases such as", "references": ["asthma", "exercise-induced asthma", "chronic obstructive asthma", "chronic obstructive asthma with status asthmaticus", "chronic obstructive asthma with acute exacerbation", "bronchial hyperreactivity", "Exercise induced asthma", "Asthma", "asthma brionchiole", "obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene Restrictive dermopathy has a genetic association with diseases such as", "references": ["ZMPSTE24", "FACE-1", "FACE1", "HGPS", "PRO1", "STE24", "Ste24p", "zinc metallopeptidase STE24"]}
-{"question": "Gene MPLKIP has a genetic association with diseases such as", "references": ["BIDS syndrome", "nonphotosensitive trichothiodystrophy", "AMISH BRITTLE HAIR BRAIN SYNDROME", "BIDS SYNDROME", "HAIR-BRAIN SYNDROME", "TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE", "Trichothiodystrophy, Nonphotosensitive 1", "Pollitt Syndrome", "TRICHOTHIODYSTROPHY 4, NONPHOTOSENSITIVE; TTD4", "TTD4", "Trichothiodystrophy-Neurocutaneous Syndrome", "nonphotosensitive trichothiodystrophy 4"]}
-{"question": "Gene hypotrichosis\u2013lymphedema\u2013telangiectasia syndrome has a genetic association with diseases such as", "references": ["SOX18", "HLTS", "HLTRS", "SRY-box 18", "SRY-box transcription factor 18"]}
-{"question": "Gene thrombocytopenia has a genetic association with diseases such as", "references": ["ANKRD26", "THC2", "bA145E8.1", "ankyrin repeat domain 26", "GATA1", "ERYF1", "GATA-1", "GF-1", "GF1", "NF-E1", "NFE1", "XLANP", "XLTDA", "XLTT", "GATA binding protein 1"]}
-{"question": "Gene OLFM4 has a genetic association with diseases such as", "references": ["amyotrophic lateral sclerosis", "ALS", "Lou Gehrig's disease", "motor neuron disease, bulbar", "Lou Gehrig disease", "Charcot disease", "Amyotrophic lateral sclerosis", "motor neurone disease", "Lou Gehrig's disease"]}
-{"question": "Gene PRKAG2 has a genetic association with diseases such as", "references": ["bipolar disorder", "BP", "manic depression", "BPAD", "kidney disease", "renal disease", "kidney damage", "kidney injury", "nephropathy", "disease of kidney", "disorder of kidney", "kidney necrosis", "nephron damage", "kidney diseases", "Wolff-Parkinson-White syndrome", "Anomalous A-V excitation", "anomalous atrioventricular excitation", "WPW syndrome", "Wolff-Parkinson-White pattern (finding)", "WPW", "Wolff-Parkinson-White pattern", "Accessory Atrioventricular Pathways", "Preexcitation Syndrome"]}
-{"question": "Gene GNAS has a genetic association with diseases such as", "references": ["colorectal cancer", "colon cancer", "rectal cancer", "large intestine cancer", "Colorectal cancer, familial", "bowel cancer", "colon and rectal cancer", "Albright's hereditary osteodystrophy", "Albright hereditary osteodystrophy", "pseudohypoparathyroidism type 1a", "PSEUDOHYPOPARATHYROIDISM, TYPE IA", "Php 1A", "PHP1A", "Albright hereditary osteodystrophy-PHP syndrome Ia", "PSEUDOHYPOPARATHYROIDISM, TYPE IA; PHP1A", "AHO-PHP syndrome Ia", "Albright Hereditary Osteodystrophy With Multiple Hormone Resistance", "pseudohypoparathyroidism Ia", "pseudohypoparathyroidism 1a", "Progressive osseous heteroplasia", "Familial ectopic ossification", "OSSEOUS HETEROPLASIA, PROGRESSIVE", "OSSEOUS HETEROPLASIA, PROGRESSIVE; POH", "Ectopic ossification familial type", "Osteoma Cutis", "Ectopic Ossification, Familial", "POH", "progressive osseous heteroplasia"]}
-{"question": "Gene Lytico-bodig disease has a genetic association with diseases such as", "references": ["TRPM7", "ALSPDC", "CHAK", "CHAK1", "LTRPC7", "LTrpC-7", "TRP-PLIK", "transient receptor potential cation channel subfamily M member 7"]}
-{"question": "Gene hyperprolactinemia has a genetic association with diseases such as", "references": ["PRLR", "PRLR", "HPRL", "MFAB", "hPRLrI", "prolactin receptor", "RI-PRLR"]}
-{"question": "Gene HOXD10 has a genetic association with diseases such as", "references": ["amyotrophic lateral sclerosis", "ALS", "Lou Gehrig's disease", "motor neuron disease, bulbar", "Lou Gehrig disease", "Charcot disease", "Amyotrophic lateral sclerosis", "motor neurone disease", "Lou Gehrig's disease", "Rocker bottom foot", "congenital vertical talus", "CVT", "Congenital convex foot", "Vertical talus", "Congenital convex pes valgus", "Rocker-bottom foot deformity", "Rocker-Bottom Foot", "VERTICAL TALUS, CONGENITAL; CVT", "Pes Valgus, Congenital Convex", "VERTICAL TALUS, CONGENITAL", "Congenital rocker-bottom foot"]}
-{"question": "Gene Fowler syndrome has a genetic association with diseases such as", "references": ["FLVCR2", "C14orf58", "CCT", "EPV", "FLVCRL14q", "MFSD7C", "PVHH", "feline leukemia virus subgroup C cellular receptor family member 2", "SLC49A2", "FLVCR heme transporter 2"]}
-{"question": "Gene MEDNIK syndrome has a genetic association with diseases such as", "references": ["AP1S1", "AP19", "CLAPS1", "EKV3", "MEDNIK", "SIGMA1A", "WUGSC:H_DJ0747G18.2", "adaptor related protein complex 1 sigma 1 subunit", "adaptor related protein complex 1 subunit sigma 1"]}
-{"question": "Gene TSBP1 has a genetic association with diseases such as", "references": ["liver cirrhosis", "cirrhosis of liver", "cirrhosis of the liver", "cirrhosis", "hepatitis C", "hep C", "NANBH", "Viral hepatitis C", "chronic hepatitis C", "hepatitis C infection", "hepatitis nonA nonB", "Non-A, Non-B Hepatitis", "hepatitis type C", "HCV", "obesity", "corpulence", "overfatness", "fatness", "obese", "atopic dermatitis", "Allergic (intrinsic) eczema (disorder)", "Atopic dermatitis", "Atopic dermatitis (disorder)", "Atopic dermatitis NOS (disorder)", "Atopic neurodermatitis (disorder)", "Besnier's prurigo", "Besnier's prurigo (disorder)", "allergic dermatitis", "atopic eczema", "atopic dermatitis and related conditions", "Atopic neurodermatitis", "Allergic", "multiple sclerosis", "MS", "encephalomyelitis disseminata", "insular sclerosis", "disseminated sclerosis", "generalized multiple sclerosis", "Generalized multiple sclerosis (disorder)", "generalised multiple sclerosis", "Multiple sclerosis; MS", "Multiple sclerosis", "asthma", "exercise-induced asthma", "chronic obstructive asthma", "chronic obstructive asthma with status asthmaticus", "chronic obstructive asthma with acute exacerbation", "bronchial hyperreactivity", "Exercise induced asthma", "Asthma", "asthma brionchiole"]}
-{"question": "Gene BTBD1 has a genetic association with diseases such as", "references": ["Kawasaki disease", "Kawasaki's disease", "MLNS", "acute febrile MCLS", "acute febrile mucocutaneous lymph node syndrome [MCLS]", "mucocutaneous lymph node syndrome", "Kawasaki disease, KD", "acute febrile mucocutaneous lymph node syndrome", "Infantile Polyarteritis Nodosa", "KAWASAKI DISEASE", "Kd", "Infantile Polyarteritis"]}
-{"question": "Gene short-chain acyl-coenzyme A dehydrogenase deficiency has a genetic association with diseases such as", "references": ["ACADS", "acyl-CoA dehydrogenase, C-2 to C-3 short chain", "ACAD3", "SCAD", "acyl-CoA dehydrogenase short chain"]}
-{"question": "Gene KCNQ5 has a genetic association with diseases such as", "references": ["refractive error", "disorder of refraction", "eye refraction disorder", "refractive disorder", "ametropia", "refraction or accommodation disorder", "refraction error", "Abnormality of refraction", "Refractive errors"]}
-{"question": "Gene Christianson syndrome has a genetic association with diseases such as", "references": ["SLC9A6", "MRSA", "NHE6", "solute carrier family 9 member A6", "MRXSCH"]}
-{"question": "Gene CEBPA has a genetic association with diseases such as", "references": ["acute myeloid leukemia", "AML - acute Myeloid Leukemia", "Leukemia, Myelocytic, acute", "acute myeloblastic leukemia", "acute myelogenous leukemia", "Acute myelogenous leukemia; AML", "Acute Granulocytic Leukemia", "LEUKEMIA, ACUTE MYELOID; AML", "Acute non lymphoblastic leukemia", "myeloid leukemia, acute", "LEUKEMIA, ACUTE MYELOID", "ANLL", "Hematopoeitic - Acute Myleogenous Leukemia (AML)", "Acute Myeloid Leukemia", "Leukemia, Acute Myeloid, Susceptibility to", "Acute Myeloid Leukemia (AML)", "Leukemia, Acute Myelogenous", "Acute Myelogenous Leukemias", "AML", "Acute Nonlymphocytic Leukemia", "Acute Myelocytic Leukemia", "acute myeloid leukaemia"]}
-{"question": "Gene ERAP1 has a genetic association with diseases such as", "references": ["ankylosing spondylitis", "Bechterew's disease", "Marie-Str\u00fcmpell disease", "Bekhterev syndrome", "Bekhterev's disease", "Marie-Strumpell disease", "Spondylarthritis ankylopoietica", "ankylosing spondylarthritis", "ankylosing spondylarthritides"]}
-{"question": "Gene DDX3X has a genetic association with diseases such as", "references": ["X-linked intellectual disability", "syndromic X-linked intellectual disability", "syndromic X-linked mental retardation", "syndromic intellectual disability, X-linked", "Mental Retardation, X-Linked"]}
-{"question": "Gene SIL1 has a genetic association with diseases such as", "references": ["Marinesco-Sjogren syndrome", "Marinesco-Sjogren syndrome", "Garland-Moorhouse syndrome", "Marinesco-Garland syndrome", "hereditary oligophrenic cerebello-lental degeneration", "MARINESCO-SJOGREN SYNDROME; MSS", "MSS", "Marinesco-Sj\u00f6gren syndrome", "Oligophrenic cerebellolenticular degeneration", "Hereditary cerebellar ataxia-childhood cataracts"]}
-{"question": "Gene IL1RL1 has a genetic association with diseases such as", "references": ["asthma", "exercise-induced asthma", "chronic obstructive asthma", "chronic obstructive asthma with status asthmaticus", "chronic obstructive asthma with acute exacerbation", "bronchial hyperreactivity", "Exercise induced asthma", "Asthma", "asthma brionchiole"]}
-{"question": "Gene MTHFD1L has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease", "coronary artery disease", "CAD", "atherosclerotic heart disease", "coronary heart disease", "ischemic heart disease", "IHD", "atherosclerotic cardiovascular disease", "CHD (coronary heart disease)", "coronary arteriosclerosis", "CHD", "coronary artery arteriosclerosis (disease)", "atherosclerosis of coronary artery", "Coronary Atherosclerosis"]}
-{"question": "Gene ATG3 has a genetic association with diseases such as", "references": ["asthma", "exercise-induced asthma", "chronic obstructive asthma", "chronic obstructive asthma with status asthmaticus", "chronic obstructive asthma with acute exacerbation", "bronchial hyperreactivity", "Exercise induced asthma", "Asthma", "asthma brionchiole"]}
-{"question": "Gene CREB5 has a genetic association with diseases such as", "references": ["attention deficit hyperactivity disorder", "ADHD", "hyperkinetic disorder", "attention deficit disorder", "AD/HD", "A.D.H.D", "attention deficit/hyperactivity disorder", "attention deficit hyperactivity syndrome", "Attention Deficit Disorder with Hyperactivity", "ADDH"]}
-{"question": "Gene chronic mucocutaneous candidiasis has a genetic association with diseases such as", "references": ["CLEC7A", "BGR", "CANDF4", "CLECSF12", "DECTIN1", "CD369", "SCARE2", "C-type lectin domain family 7 member A", "C-type lectin domain containing 7A", "TRAF3IP2", "ACT1", "C6orf2", "C6orf4", "C6orf5", "C6orf6", "CANDF8", "CIKS", "PSORS13", "TRAF3 interacting protein 2", "IL17RC", "IL17-RL", "IL17RL", "CANDF9", "interleukin 17 receptor C", "STAT1", "CANDF7", "IMD31A", "IMD31B", "IMD31C", "ISGF-3", "STAT91", "signal transducer and activator of transcription 1", "IL17RA", "CANDF5", "CD217", "CDw217", "IL-17RA", "IL17R", "hIL-17R", "interleukin 17 receptor A", "IMD51", "CARD9", "CANDF2", "hCARD9", "caspase recruitment domain family member 9"]}
-{"question": "Gene neutropenia has a genetic association with diseases such as", "references": ["ELANE", "ELA2", "GE", "HLE", "HNE", "NE", "PMN-E", "SCN1", "elastase, neutrophil expressed"]}
-{"question": "Gene SLC6A8 has a genetic association with diseases such as", "references": ["creatine transporter deficiency", "SLC6A8 deficiency", "cerebral creatine deficiency syndrome 1", "X-linked creatine transporter deficiency", "CCDS1", "Creatine Deficiency Syndrome, X-Linked", "Creatine Transporter Defect", "CEREBRAL CREATINE DEFICIENCY SYNDROME 1; CCDS1", "Cerebral Creatine Deficiency Syndrome type 1", "Creatine transporter deficiency", "Mental Retardation, X-Linked, With Creatine Transport Deficiency", "Mental Retardation, X-Linked, With Seizures, Short Stature, and Midface Hypoplasia", "X-linked creatine deficiency", "X-linked creatine deficiency syndrome"]}
-{"question": "Gene TMTC2 has a genetic association with diseases such as", "references": ["prostate cancer", "malignant tumor of the prostate", "prostatic cancer", "tumor of the prostate", "malignant neoplasm of the prostate", "prostate cancer, familial", "hereditary prostate cancer"]}
-{"question": "Gene SH3GL2 has a genetic association with diseases such as", "references": ["Parkinson's disease", "paralysis agitans", "parkinsonismus idiopathicus", "Parkinson", "Parkinson disease"]}
-{"question": "Gene SLC7A7 has a genetic association with diseases such as", "references": ["lysinuric protein intolerance", "LPI", "dibasic amino aciduria II", "hyperdibasic aminoaciduria", "familial protein intolerance", "Dibasic aminoaciduria 2", "LYSINURIC PROTEIN INTOLERANCE", "Hyperdibasic aminoaciduria type 2", "LYSINURIC PROTEIN INTOLERANCE; LPI", "Dibasic Amino Aciduria 2", "Dibasicamino aciduria II"]}
-{"question": "Gene familial hemiplegic migraine has a genetic association with diseases such as", "references": ["CACNA1A", "APCA", "BI", "CACNL1A4", "CAV2.1", "EA2", "FHM", "HPCA", "MHP", "MHP1", "SCA6", "Cav2.1", "calcium voltage-gated channel subunit alpha1 A", "EIEE42", "DEE42", "SCN1A", "EIEE6", "FEB3", "FEB3A", "FHM3", "GEFSP2", "HBSCI", "NAC1", "Nav1.1", "SCN1", "SMEI", "sodium voltage-gated channel alpha subunit 1", "DRVT", "DEE6", "DEE6A", "DEE6B", "ATP1A2", "FHM2", "MHP2", "ATPase Na+/K+ transporting subunit alpha 2", "DEE98", "FARIMPD"]}
-{"question": "Gene RORA has a genetic association with diseases such as", "references": ["schizophrenia", "Morel-Kraepelin disease", "Kraepelin-Morel disease", "dementia pr\u00e6cox", "dementia praecox", "schizophrenia-1", "asthma", "exercise-induced asthma", "chronic obstructive asthma", "chronic obstructive asthma with status asthmaticus", "chronic obstructive asthma with acute exacerbation", "bronchial hyperreactivity", "Exercise induced asthma", "Asthma", "asthma brionchiole", "mental depression", "depression"]}
-{"question": "Gene PCDH11X has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene SYNPO2 has a genetic association with diseases such as", "references": ["amyotrophic lateral sclerosis", "ALS", "Lou Gehrig's disease", "motor neuron disease, bulbar", "Lou Gehrig disease", "Charcot disease", "Amyotrophic lateral sclerosis", "motor neurone disease", "Lou Gehrig's disease"]}
-{"question": "Gene EPAS1 has a genetic association with diseases such as", "references": ["renal cell carcinoma", "RCC", "adenocarcinoma of kidney", "hypernephroma (disorder)", "hypernephroma", "Adenocarcinoma of the Kidney", "Kidney Adenocarcinoma", "Renal cell carcinoma, NOS", "Renal Cell Cancer", "Renal Cell Carcinoma", "Renal Cell Carcinoma, Stage Unspecified", "Renal Cell Adenocarcinoma", "CARCINOMA, RENAL CELL, MALIGNANT", "carcinoma, renal cell", "Peritoneal cavity"]}
-{"question": "Gene intestinal pseudo-obstruction has a genetic association with diseases such as", "references": ["ACTG2", "ACT", "ACTA3", "ACTE", "ACTL3", "ACTSG", "VSCM", "actin, gamma 2, smooth muscle, enteric", "actin gamma 2, smooth muscle", "VSCM1", "MMIHS5"]}
-{"question": "Gene SMOC2 has a genetic association with diseases such as", "references": ["vitiligo", "el morenito ojos claros"]}
-{"question": "Gene ABCB5 has a genetic association with diseases such as", "references": ["dental caries", "dental caries extending into pulp", "dental caries of smooth surface", "dental caries pit and fissure", "tooth decay", "cavities", "caries"]}
-{"question": "Gene GATA3 has a genetic association with diseases such as", "references": ["rheumatoid arthritis", "Arthritis or polyarthritis, rheumatic", "atrophic Arthritis", "Rheumatoid arthritis with vasculitis", "Malignant rheumatoid arthritis", "Rheumatoid arthritis", "acute lymphocytic leukemia", "ALL", "acute lymphoblastic leukemia", "acute lymphoblastic leukaemia", "Hodgkin lymphoma", "HL", "Hodgkin disease", "Hodgkin's sarcoma", "Hodgkins lymphoma", "stage I Subdiaphragmatic Hodgkin Lymphoma", "stage II Subdiaphragmatic Hodgkin Lymphoma", "Hodgkin's lymphoma; HL", "Hodgkin's disease", "Hodgkin's lymphoma", "hypoparathyroidism-deafness-renal disease syndrome", "Barakat syndrome", "HDR syndrome", "hypoparathyroidism, sensorineural deafness, and renal disease", "HYPOPARATHYROIDISM, SENSORINEURAL DEAFNESS, AND RENAL DISEASE; HDR", "Nephrosis, Nerve Deafness, and Hypoparathyroidism", "Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome", "HDR", "Hypoparathyroidism, Deafness, and Renal Anomalies Syndrome"]}
-{"question": "Gene SRCAP has a genetic association with diseases such as", "references": ["Floating-Harbor syndrome", "Pelletier\u2013Leisti syndrome,", "Short stature with delayed bone age, expressive language delay, a triangular face with a prominent nose and deep-set eyes", "FLOATING-HARBOR SYNDROME; FLHS", "FLOATING-HARBOR SYNDROME", "FHS", "FLHS", "Pelletier-Leisti syndrome"]}
-{"question": "Gene SELPLG has a genetic association with diseases such as", "references": ["conduct disorder", "disruptive behavior disorder"]}
-{"question": "Gene achondrogenesis has a genetic association with diseases such as", "references": ["TRIP11", "ACG1A", "CEV14", "GMAP-210", "TRIP-11", "TRIP230", "GMAP210", "thyroid hormone receptor interactor 11", "ODCD", "ODCD1", "SLC26A2", "D5S1708", "DTD", "DTDST", "EDM4", "MST153", "MSTP157", "solute carrier family 26 member 2"]}
-{"question": "Gene COMP has a genetic association with diseases such as", "references": ["pseudoachondroplasia", "SPONDYLOEPIPHYSEAL DYSPLASIA, PSEUDOACHONDROPLASTIC", "pseudoachondroplastic dysplasia", "PSEUDOACHONDROPLASIA; PSACH", "PSACH", "Pseudoachondroplastic spondyloepiphyseal dysplasia", "Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome", "PSEUDOACHONDROPLASIA"]}
-{"question": "Gene Holt-Oram syndrome has a genetic association with diseases such as", "references": ["TBX5", "HOS", "T-box 5", "T-box transcription factor 5"]}
-{"question": "Gene McGillivray syndrome has a genetic association with diseases such as", "references": ["FGFR2", "BBDS", "BEK", "BFR-1", "CD332", "CEK3", "CFD1", "ECT1", "JWS", "K-SAM", "KGFR", "TK14", "TK25", "fibroblast growth factor receptor 2"]}
-{"question": "Gene atrioventricular septal defect has a genetic association with diseases such as", "references": ["GATA6", "GATA binding protein 6", "GJA1", "AVSD3", "CMDR", "CX43", "EKVP", "GJAL", "HLHS1", "HSS", "ODDD", "PPKCA", "gap junction protein alpha 1", "EKVP3", "GATA4", "GATA binding protein 4", "ASD2", "TACHD", "VSD1", "TOF"]}
-{"question": "Gene VPS13B has a genetic association with diseases such as", "references": ["Cohen syndrome", "COHEN SYNDROME", "Pepper Syndrome", "COH1", "Chs1", "Cutis Verticis Gyrata, Retinitis Pigmentosa, and Sensorineural Deafness", "COHEN SYNDROME; COH1", "Coh", "Chs1, Formerly", "Hypotonia, Obesity, and Prominent Incisors"]}
-{"question": "Gene Cant\u00fa syndrome has a genetic association with diseases such as", "references": ["ABCC9", "ABC37", "ATFB12", "CANTU", "CMD1O", "SUR2", "ATP binding cassette subfamily C member 9", "KCNJ8", "KIR6.1", "uKATP-1", "potassium voltage-gated channel subfamily J member 8", "potassium inwardly rectifying channel subfamily J member 8"]}
-{"question": "Gene UNC13C has a genetic association with diseases such as", "references": ["smallpox", "ordinary smallpox", "variola", "variola vera"]}
-{"question": "Gene CAPZB has a genetic association with diseases such as", "references": ["Crohn's disease", "regional enteritis", "Crohn disease", "Crohn's disease of colon (disorder)", "Crohn's disease of large bowel", "Granulomatous Colitis", "regional Ileitis", "regional colitis", "regional enteritis of small intestine with large intestine", "regional enteritis of the large bowel", "regional ileocolitis", "Crohn's disease of colon", "Crohn", "psoriasis"]}
-{"question": "Gene FLNB has a genetic association with diseases such as", "references": ["Boomerang dysplasia", "Dwarfism with short, bowed, rigid limbs and characteristic facies", "BOOMERANG DYSPLASIA", "Boomerang-like skeletal dysplasia", "Larsen syndrome", "dominant larsen syndrome", "LARSEN SYNDROME; LRS", "LARSEN SYNDROME", "Autosomal dominant Larsen syndrome", "LRS"]}
-{"question": "Gene NCS1 has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene PSMA4 has a genetic association with diseases such as", "references": ["rheumatoid arthritis", "Arthritis or polyarthritis, rheumatic", "atrophic Arthritis", "Rheumatoid arthritis with vasculitis", "Malignant rheumatoid arthritis", "Rheumatoid arthritis"]}
-{"question": "Gene MAGI2 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene sick sinus syndrome has a genetic association with diseases such as", "references": ["MYH6", "ASD3", "CMD1EE", "CMH14", "MYHC", "MYHCA", "SSS3", "alpha-MHC", "myosin, heavy chain 6, cardiac muscle, alpha", "myosin heavy chain 6", "SCN5A", "CDCD2", "CMD1E", "CMPD2", "HB1", "HB2", "HBBD", "HH1", "ICCD", "IVF", "LQT3", "Nav1.5", "PFHB1", "SSS1", "VF1", "sodium voltage-gated channel alpha subunit 5", "HCN4", "SSS2", "hyperpolarization activated cyclic nucleotide gated potassium channel 4", "BRGDA8", "EIG18"]}
-{"question": "Gene FOXG1 has a genetic association with diseases such as", "references": ["Rett syndrome", "Rett's disorder", "cerebroatrophic hyperammonemia", "atypical Rett syndrome", "Rett's syndrome"]}
-{"question": "Gene Saethre-Chotzen syndrome has a genetic association with diseases such as", "references": ["FGFR2", "BBDS", "BEK", "BFR-1", "CD332", "CEK3", "CFD1", "ECT1", "JWS", "K-SAM", "KGFR", "TK14", "TK25", "fibroblast growth factor receptor 2"]}
-{"question": "Gene NOS2 has a genetic association with diseases such as", "references": ["psoriasis"]}
-{"question": "Gene PEX3 has a genetic association with diseases such as", "references": ["Zellweger spectrum disorder", "Peroxisomal Biogenesis Disorders", "Zellweger Syndrome Spectrum", "Cerebrohepatorenal Syndrome", "ZSS", "Peroxisome biogenesis disorders-Zellweger spectrum disorders", "peroxisome biogenesis disorder", "peroxisome biogenesis disorders, Zellweger syndrome spectrum", "PBD-ZSD", "Zellweger syndrome spectrum", "Peroxisome biogenesis disorder spectrum", "ZSD", "Zellweger spectrum", "PBD, ZSS", "cerebrohepatorenal syndrome", "Zellweger spectrum disorder", "Peroxisome biogenesis disorder", "obsolete Zellweger spectrum disorder"]}
-{"question": "Gene Ichthyosis follicularis with alopecia and photophobia syndrome has a genetic association with diseases such as", "references": ["MBTPS2", "BRESEK", "IFAP", "KFSD", "KFSDX", "OLMSX", "S2P", "membrane bound transcription factor peptidase, site 2", "OI19"]}
-{"question": "Gene Charcot\u2013Marie\u2013Tooth disease has a genetic association with diseases such as", "references": ["PMP22", "CMT1A", "CMT1E", "DSS", "GAS-3", "HMSNIA", "HNPP", "Sujojp110", "GAS3", "peripheral myelin protein 22", "CIDP", "Sp110", "GJB1", "CMTX", "CMTX1", "CX32", "gap junction protein beta 1", "MPZ", "CHM", "CMT1", "CMT1B", "CMT2I", "CMT2J", "CMT4E", "CMTDI3", "CMTDID", "DSS", "HMSNIB", "MPP", "P0", "myelin protein zero", "CHN2"]}
-{"question": "Gene EBF1 has a genetic association with diseases such as", "references": ["breast cancer", "malignant neoplasm of breast", "malignant tumor of the breast", "mammary cancer", "primary breast cancer", "breast disorder", "obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene coenzyme Q10 deficiency disease has a genetic association with diseases such as", "references": ["COQ2", "CL640", "COQ10D1", "MSA1", "PHB:PPT", "coenzyme Q2, polyprenyltransferase"]}
-{"question": "Gene NEDD4L has a genetic association with diseases such as", "references": ["amyotrophic lateral sclerosis", "ALS", "Lou Gehrig's disease", "motor neuron disease, bulbar", "Lou Gehrig disease", "Charcot disease", "Amyotrophic lateral sclerosis", "motor neurone disease", "Lou Gehrig's disease"]}
-{"question": "Gene major depressive disorder has a genetic association with diseases such as", "references": ["CACNA1C", "CACH2", "CACN2", "CACNL1A1", "CCHL1A1", "CaV1.2", "LQT8", "TS", "calcium voltage-gated channel subunit alpha1 C", "TS. LQT8", "CCBE1", "HKLLS1", "collagen and calcium binding EGF domains 1", "MYO10", "myosin X", "ITGA11", "HsT18964", "integrin subunit alpha 11", "ENOX1", "CNOX", "PIG38", "bA64J21.1", "cCNOX", "ecto-NOX disulfide-thiol exchanger 1", "KCNH5", "EAG2", "H-EAG2", "Kv10.2", "hEAG2", "potassium voltage-gated channel subfamily H member 5", "ESRRG", "ERR3", "ERRgamma", "NR3B3", "estrogen related receptor gamma", "ERRg", "ERR-gamma", "TRPS1", "GC79", "LGCR", "transcriptional repressor GATA binding 1", "PCLO", "ACZ", "PCH3", "piccolo presynaptic cytomatrix protein", "FAT4", "CDHF14", "CDHR11", "FAT-J", "FATJ", "NBLA00548", "VMLDS2", "HKLLS2", "FAT atypical cadherin 4", "SYNE1", "8B", "ARCA1", "C6orf98", "CPG2", "EDMD4", "MYNE1", "Nesp1", "SCAR8", "dJ45H2.2", "spectrin repeat containing nuclear envelope protein 1", "KASH1", "AMCM", "AMC3", "ANK3", "ANKYRIN-G", "MRT37", "ankyrin 3, node of Ranvier (ankyrin G)", "ankyrin 3", "SP4", "HF1B", "SPR-1", "Sp4 transcription factor"]}
-{"question": "Gene Ichthyosis hystrix has a genetic association with diseases such as", "references": ["KRT1", "CK1", "EHK", "EHK1", "EPPK", "K1", "KRT1A", "NEPPK", "keratin 1"]}
-{"question": "Gene LBP has a genetic association with diseases such as", "references": ["periodontitis", "pyorrhea", "chronic pericementitis", "periodontium inflammation", "periodontiumitis"]}
-{"question": "Gene REL has a genetic association with diseases such as", "references": ["rheumatoid arthritis", "Arthritis or polyarthritis, rheumatic", "atrophic Arthritis", "Rheumatoid arthritis with vasculitis", "Malignant rheumatoid arthritis", "Rheumatoid arthritis", "psoriatic arthritis", "arthritis psoriatica", "arthropathic psoriasis", "psoriatic arthropathy", "Arthritis, Psoriatic"]}
-{"question": "Gene Arthrogryposis\u2013renal dysfunction\u2013cholestasis syndrome has a genetic association with diseases such as", "references": ["VPS33B", "VPS33B, late endosome and lysosome associated", "VPS33B late endosome and lysosome associated", "VIPAS39", "C14orf133", "SPE-39", "SPE39", "VIPAR", "VPS16B", "hSPE-39", "VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog"]}
-{"question": "Gene Fleck corneal dystrophy has a genetic association with diseases such as", "references": ["PIKFYVE", "CFD", "FAB1", "HEL37", "PIP5K", "PIP5K3", "ZFYVE29", "phosphoinositide kinase, FYVE-type zinc finger containing"]}
-{"question": "Gene exanthem has a genetic association with diseases such as", "references": ["CCHCR1", "C6orf18", "HCR", "SBP", "coiled-coil alpha-helical rod protein 1", "pg8", "POLR3G", "RPC32", "RPC7", "polymerase (RNA) III subunit G", "RNA polymerase III subunit G", "C31"]}
-{"question": "Gene TNRC6B has a genetic association with diseases such as", "references": ["prostate cancer", "malignant tumor of the prostate", "prostatic cancer", "tumor of the prostate", "malignant neoplasm of the prostate", "prostate cancer, familial", "hereditary prostate cancer", "uterine fibroid", "UTERUS FIBROMA", "leiomyoma of Corpus Uteri", "uterine leiomyoma", "plexiform leiomyoma"]}
-{"question": "Gene Torsion dystonia has a genetic association with diseases such as", "references": ["TOR1A", "DQ2", "DYT1", "Torsin A", "torsin family 1 member A", "AMC5"]}
-{"question": "Gene CAMK1D has a genetic association with diseases such as", "references": ["q", "nhac", "obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene STK11 has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene CLN5 has a genetic association with diseases such as", "references": ["neuronal ceroid lipofuscinosis", "hereditary ceroid lipofuscinosis", "neuronal ceroid lipofuscinosis (disorder)", "NCL"]}
-{"question": "Gene INPP5D has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene PQBP1 has a genetic association with diseases such as", "references": ["Renpenning syndrome", "Golabi-Ito-Hall syndrome", "Sutherland-Haan X-linked mental retardation syndrome", "X-linked intellectual disability due to PQBP1 mutations", "X-linked intellectual disability, Renpenning type", "X-linked mental retardation Renpenning type", "X-linked mental retardation with spastic diplegia", "syndromic X-linked mental retardation 8", "Mental Retardation, X-Linked, Syndromic 8", "Mental Retardation, X-Linked, With Spastic Diplegia", "RENPENNING SYNDROME 1", "Mental Retardation, X-Linked 55", "Renpenning Syndrome type 1", "RENPENNING SYNDROME 1; RENS1", "Mental Retardation, X-Linked, Syndromic 3", "RENS1", "Mental Retardation, X-Linked, Renpenning Type"]}
-{"question": "Gene Schindler disease has a genetic association with diseases such as", "references": ["NAGA", "D22S674", "GALB", "alpha-N-acetylgalactosaminidase"]}
-{"question": "Gene FMO3 has a genetic association with diseases such as", "references": ["Trimethylaminuria", "fish odor syndrome", "TMAU", "TRIMETHYLAMINURIA; TMAU", "Fish-Odor Syndrome", "trimethylaminuria", "fish-odor syndrome"]}
-{"question": "Gene PRDM16 has a genetic association with diseases such as", "references": ["migraine", "migraine variant", "sick headache", "migraine with or without aura", "migraine disorders", "migraine disorder"]}
-{"question": "Gene TRIO has a genetic association with diseases such as", "references": ["peripheral neuropathy", "neuropathy", "peripheral nervous system disease", "peripheral nerve disease", "peripheral neuropathy", "perpheral nervous system diseases", "Peripheral Nervous System Diseases", "\u30cb\u30e5\u30fc\u30ed\u30d1\u30b7\u30fc"]}
-{"question": "Gene GDNF has a genetic association with diseases such as", "references": ["phaeochromocytoma", "PCC", "adrenal gland pheochromocytoma", "PHEOCHROMOCYTOMA", "Pheochromocytoma, Susceptibility to", "Pheochromocytoma"]}
-{"question": "Gene MEIS1 has a genetic association with diseases such as", "references": ["restless legs syndrome", "WED", "Willis-Ekbom disease", "Wittmaack-Ekbom syndrome", "RLS", "Restless Leg Syndrome"]}
-{"question": "Gene nonsyndromic deafness has a genetic association with diseases such as", "references": ["WHRN", "CIP98", "PDZD7B", "USH2D", "WI", "DFNB31", "whirlin", "USH1G", "ANKS4A", "SANS", "USH1 protein network component sans", "TNC", "150-225", "DFNA56", "GMEM", "GP", "HXB", "JI", "TN", "TN-C", "Tenascin C", "ACTG1", "ACT", "ACTG", "BRWS2", "DFNA20", "DFNA26", "HEL-176", "actin gamma 1", "CDH23", "CDHR23", "USH1D", "cadherin-related 23", "cadherin related 23", "PITA5", "CLDN14", "DFNB29", "claudin 14", "COCH", "COCH-5B2", "COCH5B2", "DFNA9", "cochlin", "DFNB110", "ESRRB", "DFNB35", "ERR2", "ERRb", "ESRL2", "NR3B2", "estrogen related receptor beta", "ERRbeta2", "ERR beta-2", "Esrrb", "EYA4", "CMD1J", "DFNA10", "EYA transcriptional coactivator and phosphatase 4", "GIPC3", "C19orf64", "DFNB15", "DFNB72", "DFNB95", "GIPC PDZ domain containing family member 3", "GRXCR1", "DFNB25", "PPP1R88", "glutaredoxin and cysteine rich domain containing 1", "LHFPL5", "DFNB67", "TMHS", "dJ510O8.8", "lipoma HMGIC fusion partner-like 5", "LHFPL tetraspan subfamily member 5", "LOXHD1", "DFNB77", "LH2D1", "lipoxygenase homology domains 1", "lipoxygenase homology PLAT domains 1", "MARVELD2", "DFNB49", "MARVD2", "MRVLDC2", "Tric", "MARVEL domain containing 2", "MYH14", "DFNA4", "DFNA4A", "MHC16", "MYH17", "NMHC II-C", "NMHC-II-C", "PNMHH", "myosin", "FP17425", "myosin, heavy chain 14, non-muscle", "myosin heavy chain 14", "MYO15A", "DFNB3", "MYO15", "myosin XVA", "MYO6", "DFNA22", "DFNB37", "myosin VI", "Myo6-008", "Myo6-007", "MYO7A", "DFNA11", "DFNB2", "MYOVIIA", "MYU7A", "NSRD2", "USH1B", "myosin VIIA", "OTOG", "DFNB18B", "MLEMP", "OTGN", "otogelin", "POU3F4", "BRAIN-4", "BRN-4", "BRN4", "DFN3", "DFNX2", "OCT-9", "OTF-9", "OTF9", "POU class 3 homeobox 4", "POU4F3", "BRN3C", "DFNA15", "POU class 4 homeobox 3", "DFNA42", "DFNA52", "RDX", "DFNB24", "radixin", "STRC", "DFNB16", "stereocilin", "TECTA", "DFNA12", "DFNA8", "DFNB21", "tectorin alpha", "TMC1", "DFNA36", "DFNB11", "DFNB7", "transmembrane channel like 1", "TMPRSS3", "DFNB10", "DFNB8", "ECHOS1", "TADG12", "transmembrane protease, serine 3", "transmembrane serine protease 3"]}
-{"question": "Gene B3GAT2 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene TBX19 has a genetic association with diseases such as", "references": ["adrenocorticotropic hormone deficiency", "ACTH DEFICIENCY, ISOLATED", "ACTH DEFICIENCY, ISOLATED; IAD", "IAD", "Congenital isolated ACTH deficiency", "Adrenocorticotropic Hormone Deficiency"]}
-{"question": "Gene Rapp-Hodgkin syndrome has a genetic association with diseases such as", "references": ["TP63", "AIS", "B(p51A)", "B(p51B)", "EEC3", "KET", "LMS", "NBP", "OFC8", "RHS", "SHFM4", "TP53CP", "TP53L", "TP73L", "p40", "p51", "p53CP", "p63", "p73H", "p73L", "tumor protein p63"]}
-{"question": "Gene NTNG1 has a genetic association with diseases such as", "references": ["q", "nhac"]}
-{"question": "Gene BTNL2 has a genetic association with diseases such as", "references": ["multiple sclerosis", "MS", "encephalomyelitis disseminata", "insular sclerosis", "disseminated sclerosis", "generalized multiple sclerosis", "Generalized multiple sclerosis (disorder)", "generalised multiple sclerosis", "Multiple sclerosis; MS", "Multiple sclerosis", "hepatitis C", "hep C", "NANBH", "Viral hepatitis C", "chronic hepatitis C", "hepatitis C infection", "hepatitis nonA nonB", "Non-A, Non-B Hepatitis", "hepatitis type C", "HCV", "liver cirrhosis", "cirrhosis of liver", "cirrhosis of the liver", "cirrhosis", "sarcoidosis", "Boeck sarcoid", "benign lymphogranulomatosis", "Besnier-Boeck-Schaumann disease", "lymphogranulomatosis", "Sarcoidosis", "adenocarcinoma of the lung", "lung adenocarcinoma", "nonsmall cell adenocarcinoma", "adenocarcinoma of lung", "bronchogenic lung adenocarcinoma", "Adenocarcinoma of the Lung", "non-small cell lung adenocarcinoma", "pulmonary adenocarcinoma", "ulcerative colitis", "hemorrhagic colitis", "Ulcerative Colitis", "Colitis Ulcerative", "Ulcerative colitis", "left-sided ulcerative colitis", "UC"]}
-{"question": "Gene TRPC4 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene multiple system atrophy has a genetic association with diseases such as", "references": ["COQ2", "CL640", "COQ10D1", "MSA1", "PHB:PPT", "coenzyme Q2, polyprenyltransferase"]}
-{"question": "Gene restless legs syndrome has a genetic association with diseases such as", "references": ["MEIS1", "Meis homeobox 1", "BTBD9", "dJ322I12.1", "BTB domain containing 9", "PTPRD", "HPTP", "HPTPD", "HPTPDELTA", "PTPD", "RPTPDELTA", "protein tyrosine phosphatase, receptor type D", "protein tyrosine phosphatase receptor type D", "R-PTP-delta"]}
-{"question": "Gene myopia has a genetic association with diseases such as", "references": ["SNTB1", "59-DAP", "A1B", "BSYN2", "DAPA1B", "SNT2", "SNT2B1", "TIP-43", "syntrophin beta 1", "VIPR2", "C16DUPq36.3", "DUP7q36.3", "PACAP-R-3", "PACAP-R3", "VIP-R-2", "VPAC2", "VPAC2R", "VPCAP2R", "vasoactive intestinal peptide receptor 2", "CAPN9", "GC36", "nCL-4", "calpain 9", "FHIT", "AP3Aase", "FRA3B", "fragile histidine triad", "tr\u00edada histidina fr\u00e0gil", "fragile histidine triad diadenosine triphosphatase", "DHX15", "DBP1", "DDX15", "HRH2", "PRP43", "PRPF43", "PrPp43p", "DEAH-box helicase 15", "BMP6", "VGR", "VGR1", "bone morphogenetic protein 6", "SRPK2", "SFRSK2", "SRSF protein kinase 2", "PTPRN2", "IA-2beta", "IAR", "ICAAR", "PTPRP", "R-PTP-N2", "protein tyrosine phosphatase, receptor type N2", "protein tyrosine phosphatase receptor type N2", "GATA4", "GATA binding protein 4", "ASD2", "TACHD", "VSD1", "TOF", "PTPRD", "HPTP", "HPTPD", "HPTPDELTA", "PTPD", "RPTPDELTA", "protein tyrosine phosphatase, receptor type D", "protein tyrosine phosphatase receptor type D", "R-PTP-delta", "DENND1A", "FAM31A", "KIAA1608", "DENN domain containing 1A", "TACC2", "AZU-1", "ECTACC", "transforming acidic coiled-coil containing protein 2", "FLI1", "EWSR2", "SIC-1", "Fli-1 proto-oncogene, ETS transcription factor", "BDPLT21", "FLI-1", "PML", "MYL", "PP8675", "RNF71", "TRIM19", "Promyelocytic leukemia protein", "promyelocytic leukemia", "Probable transcription factor PML", "PML nuclear body scaffold", "DNAH9", "DNAH17L", "DNEL1", "DYH9", "Dnahc9", "HL-20", "HL20", "dynein axonemal heavy chain 9", "CILD40", "ZNF536", "zinc finger protein 536", "SPTBN1", "ELF", "HEL102", "SPTB2", "betaSpII", "spectrin beta, non-erythrocytic 1", "DDISBA", "PARP8", "ARTD16", "pART16", "poly(ADP-ribose) polymerase family member 8", "PRIMPOL", "CCDC111", "MYP22", "primase and DNA directed polymerase", "Primpol1", "PrimPol", "LRPAP1", "A2MRAP", "A2RAP", "HBP44", "MRAP", "MYP23", "RAP", "alpha-2-MRAP", "LDL-receptor-related protein associated protein", "LDL receptor related protein associated protein 1", "ZNF644", "BM-005", "MYP21", "NatF", "ZEP-2", "zinc finger protein 644"]}
-{"question": "Gene renal glycosuria has a genetic association with diseases such as", "references": ["SLC5A2", "SGLT2", "solute carrier family 5 member 2"]}
-{"question": "Gene SPTB has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene ADULT syndrome has a genetic association with diseases such as", "references": ["TP63", "AIS", "B(p51A)", "B(p51B)", "EEC3", "KET", "LMS", "NBP", "OFC8", "RHS", "SHFM4", "TP53CP", "TP53L", "TP73L", "p40", "p51", "p53CP", "p63", "p73H", "p73L", "tumor protein p63"]}
-{"question": "Gene acheiropody has a genetic association with diseases such as", "references": ["LMBR1", "ACHP", "C7orf2", "DIF14", "PPD2", "TPT", "ZRS", "LSS", "THYP", "limb development membrane protein 1"]}
-{"question": "Gene hypophosphatasia has a genetic association with diseases such as", "references": ["ALPL", "AP-TNAP", "APTNAP", "HOPS", "TNAP", "TNSALP", "alkaline phosphatase, liver/bone/kidney", "TNALP", "alkaline phosphatase, biomineralization associated", "HPPA", "HPPI", "HPPC", "HPPO", "TNS-ALP"]}
-{"question": "Gene dyslexia has a genetic association with diseases such as", "references": ["PCSK6", "PACE4", "SPC4", "proprotein convertase subtilisin/kexin type 6"]}
-{"question": "Gene ERBB3 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "type-1 diabetes", "IDDM", "insulin-dependent diabetes mellitus", "type I diabetes mellitus", "T1DM", "insulin dependent diabetes", "juvenile diabetes", "diabetes mellitus juvenile type", "DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM", "Diabetes Mellitus, Type 1", "Diabetes Mellitus, Insulin-Dependent, 1", "DIABETES MELLITUS, INSULIN-DEPENDENT", "Juvenile-Onset Diabetes", "Insulin-Dependent Diabetes Mellitus 1", "diabetes (type 1)", "type 1 diabetes mellitus"]}
-{"question": "Gene DAPK1 has a genetic association with diseases such as", "references": ["smallpox", "ordinary smallpox", "variola", "variola vera", "pancreatic cancer", "Ca tail of pancreas", "Ca head of pancreas", "Ca body of pancreas", "malignant neoplasm of head of pancreas", "malignant neoplasm of tail of pancreas", "malignant neoplasm of body of pancreas"]}
-{"question": "Gene CDH3 has a genetic association with diseases such as", "references": ["Hypotrichosis with juvenile macular dystrophy", "congenital hypotrichosis with juvenile macular dystrophy", "Hjmd", "hypotrichosis with cone-rod dystrophy", "HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY", "HYPOTRICHOSIS, CONGENITAL, WITH JUVENILE MACULAR DYSTROPHY; HJMD", "Hypotrichosis with juvenile macular degeneration", "EEM syndrome", "Eem Syndrome", "ECTODERMAL DYSPLASIA, ECTRODACTYLY, AND MACULAR DYSTROPHY SYNDROME", "Ectodermal dysplasia-ectrodactyly-macular dystrophy syndrome", "Ectodermal dysplasia, ectrodactyly, and macular dystrophy", "ECTODERMAL DYSPLASIA, ECTRODACTYLY, AND MACULAR DYSTROPHY SYNDROME; EEMS", "EEMS", "ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome"]}
-{"question": "Gene MASS syndrome has a genetic association with diseases such as", "references": ["FBN1", "ACMICD", "ECTOL1", "FBN", "GPHYSD2", "MASS", "MFS1", "OCTD", "SGS", "SSKS", "WMS", "WMS2", "MFLS", "fibrillin 1"]}
-{"question": "Gene LEF1 has a genetic association with diseases such as", "references": ["chronic lymphocytic leukemia", "B-cell chronic lymphocytic leukemia", "CLL", "chronic lymphatic leukemia", "lymphoplasmacytic leukemia", "B-cell chronic lymphoid leukemia", "B-Cell Chronic Lymphogenous Leukemia", "Chronic Lymphocytic Leukemia (CLL)", "Hematopoeitic - Chronic Lymphocytic Leukemia (CLL)", "Chronic B-Cell Lymphocytic Leukemia", "B-Cell CLL", "Leukemia, Chronic Lymphatic", "B Cell CLL", "Small lymphocytic lymphoma", "BCLL", "LEUKEMIA, CHRONIC LYMPHOCYTIC; CLL", "B Cell Chronic Lymphocytic Leukemia", "B-CLL", "Chronic Lymphocytic Leukemia", "B Cell Lymphocytic Leukemia", "Chronic Lymphogenous Leukemia", "B-Cell Lymphocytic Leukemia", "LEUKEMIA, CHRONIC LYMPHOCYTIC", "Chronic lymphocytic leukemia, NOS", "Chronic lymphocytic leukemia; CLL", "Leukemia, Lymphocytic, Chronic, B-Cell", "Chronic lymphocytic leukaemia", "chronic lymphocytic leukaemia", "systemic lupus erythematosus", "SLE", "lupus", "Lupus Erythematosus, systemic", "SLE - Lupus Erythematosus, systemic", "disseminated lupus erythematosus", "Systemic lupus erythematosus"]}
-{"question": "Gene aspirin-induced asthma has a genetic association with diseases such as", "references": ["TBX21", "T-PET", "T-bet", "TBET", "TBLYM", "T-box 21", "T-box transcription factor 21", "IMD88"]}
-{"question": "Gene IL2RB has a genetic association with diseases such as", "references": ["rheumatoid arthritis", "Arthritis or polyarthritis, rheumatic", "atrophic Arthritis", "Rheumatoid arthritis with vasculitis", "Malignant rheumatoid arthritis", "Rheumatoid arthritis", "tuberculosis", "hydrothorax", "Tuberculosis", "In the clinic. Tuberculosis", "TB", "phthisis", "phthisis pulmonalis", "consumption", "phtisis", "asthma", "exercise-induced asthma", "chronic obstructive asthma", "chronic obstructive asthma with status asthmaticus", "chronic obstructive asthma with acute exacerbation", "bronchial hyperreactivity", "Exercise induced asthma", "Asthma", "asthma brionchiole"]}
-{"question": "Gene RNASEL has a genetic association with diseases such as", "references": ["multiple sclerosis", "MS", "encephalomyelitis disseminata", "insular sclerosis", "disseminated sclerosis", "generalized multiple sclerosis", "Generalized multiple sclerosis (disorder)", "generalised multiple sclerosis", "Multiple sclerosis; MS", "Multiple sclerosis"]}
-{"question": "Gene GPSM1 has a genetic association with diseases such as", "references": ["type 2 diabetes", "NIDDM", "non-insulin-dependent diabetes mellitus", "type II diabetes mellitus", "Diabetes mellitus type 2", "Rare insulin-independent diabetes mellitus", "Diabetes Mellitus, Type 2", "type 2 diabetes mellitus", "diabetes (type 2)"]}
-{"question": "Gene gout has a genetic association with diseases such as", "references": ["SLC2A9", "solute carrier family 2 (facilitated glucose transporter), member 9", "GLUT9", "GLUTX", "UAQTL2", "URATv1", "solute carrier family 2 member 9", "ABCG2", "ATP-binding cassette, sub-family G (WHITE), member 2 (Junior blood group)", "ABC15", "ABCP", "BCRP", "BCRP1", "BMDP", "CD338", "CDw338", "EST157481", "GOUT1", "MRX", "MXR", "MXR1", "UAQTL1", "MXR-1", "ATP binding cassette subfamily G member 2 (Junior blood group)"]}
-{"question": "Gene PASLI Disease has a genetic association with diseases such as", "references": ["PIK3R1", "AGM7", "GRB1", "IMD36", "p85", "p85-ALPHA", "phosphoinositide-3-kinase regulatory subunit 1", "PI3KR1", "PIK3CD", "APDS", "IMD14", "P110DELTA", "PI3K", "p110D", "phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta", "IMD14B", "ROCHIS", "IMD14A"]}
-{"question": "Gene FLT3 has a genetic association with diseases such as", "references": ["acute myeloid leukemia", "AML - acute Myeloid Leukemia", "Leukemia, Myelocytic, acute", "acute myeloblastic leukemia", "acute myelogenous leukemia", "Acute myelogenous leukemia; AML", "Acute Granulocytic Leukemia", "LEUKEMIA, ACUTE MYELOID; AML", "Acute non lymphoblastic leukemia", "myeloid leukemia, acute", "LEUKEMIA, ACUTE MYELOID", "ANLL", "Hematopoeitic - Acute Myleogenous Leukemia (AML)", "Acute Myeloid Leukemia", "Leukemia, Acute Myeloid, Susceptibility to", "Acute Myeloid Leukemia (AML)", "Leukemia, Acute Myelogenous", "Acute Myelogenous Leukemias", "AML", "Acute Nonlymphocytic Leukemia", "Acute Myelocytic Leukemia", "acute myeloid leukaemia"]}
-{"question": "Gene WNT9B has a genetic association with diseases such as", "references": ["vasculitis", "Angiitis", "Vasculitis Syndrome"]}
-{"question": "Gene ABCB11 has a genetic association with diseases such as", "references": ["metabolic disease", "metabolic illness", "disorder of metabolic process", "metabolic disorder", "metabolic diseases", "disease of metabolism"]}
-{"question": "Gene CD247 has a genetic association with diseases such as", "references": ["systemic scleroderma", "scleroderma, systemic", "PSS (progressive systemic sclerosis)", "Scleroderma (& [systemic sclerosis])", "progressive systemic sclerosis", "systemic sclerosis", "Systemic sclerosis or systemic scleroderma", "Progressive systemic sclerosis", "Scleroderma syndrome", "Scleroderma", "PSS", "Systemic Scleroderma", "Scleroderma, Diffuse", "SSc", "Scleroderma, Systemic", "SSc, Diffuse Sclerosis", "Diffuse Sclerosis", "Diffuse Scleroderma", "Systemic scleroderma", "Systemic Sclerosis", "rheumatoid arthritis", "Arthritis or polyarthritis, rheumatic", "atrophic Arthritis", "Rheumatoid arthritis with vasculitis", "Malignant rheumatoid arthritis", "Rheumatoid arthritis", "coeliac disease", "celiac sprue", "celiac disease", "nontropical sprue", "endemic sprue", "gluten enteropathy", "idiopathic steatorrhea", "CeD"]}
-{"question": "Gene X-linked lymphoproliferative disease has a genetic association with diseases such as", "references": ["SH2D1A", "DSHP", "EBVS", "IMD5", "LYP", "MTCP1", "SAP", "SAP/SH2D1A", "XLP", "XLPD", "XLPD1", "SH2 domain containing 1A", "XIAP", "API3", "BIRC4", "IAP-3", "ILP1", "MIHA", "XLP2", "hIAP-3", "hIAP3", "X-linked inhibitor of apoptosis"]}
-{"question": "Gene Andersen-Tawil syndrome has a genetic association with diseases such as", "references": ["KCNJ2", "ATFB9", "HHBIRK1", "HHIRK1", "IRK1", "KIR2.1", "LQT7", "SQT3", "potassium voltage-gated channel subfamily J member 2", "potassium inwardly rectifying channel subfamily J member 2"]}
-{"question": "Gene SLC1A2 has a genetic association with diseases such as", "references": ["essential tremor", "ET", "benign tremor", "familiar tremor", "benign essential tremor", "essential hereditary tremor", "shaky hand syndrome"]}
-{"question": "Gene ICOSLG has a genetic association with diseases such as", "references": ["coeliac disease", "celiac sprue", "celiac disease", "nontropical sprue", "endemic sprue", "gluten enteropathy", "idiopathic steatorrhea", "CeD"]}
-{"question": "Gene RORC has a genetic association with diseases such as", "references": ["inflammatory bowel diseases", "IBD", "inflammatory bowel disease"]}
-{"question": "Gene SIX3 has a genetic association with diseases such as", "references": ["schizencephaly"]}
-{"question": "Gene Localized epidermolysis bullosa simplex has a genetic association with diseases such as", "references": ["KRT14", "CK14", "EBS3", "EBS4", "K14", "NFJ", "keratin 14", "EBS1D", "EBS1", "EBS1B", "EBS1A", "EBS1C", "ITGB4", "CD104", "GP150", "integrin subunit beta 4", "KRT5", "CK5", "DDD", "DDD1", "EBS2", "K5", "KRT5A", "keratin 5", "EBS2E", "EBS2B", "EBS2C", "EBS1", "EBS2A", "EBS2F", "EBS2D"]}
-{"question": "Gene ATP8B3 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene metabolic disease has a genetic association with diseases such as", "references": ["G6PC2", "IGRP", "glucose-6-phosphatase catalytic subunit 2", "CAMK2B", "CAM2", "CAMK2", "CAMKB", "calcium/calmodulin dependent protein kinase II beta", "MRD54", "CaMKIIbeta", "GALNT2", "GalNAc-T2", "polypeptide N-acetylgalactosaminyltransferase 2", "CDG2T", "APOB", "FLDB", "LDLCQ4", "apoB-100", "apoB-48", "apolipoprotein B", "FCHL2", "NR1H3", "LXR-a", "LXRA", "RLD-1", "Liver X receptor alpha", "nuclear receptor subfamily 1 group H member 3", "PPP4R3B", "FLFL2", "PP4R3B", "PSY2", "smk1", "SMEK2", "protein phosphatase 4 regulatory subunit 3B", "GCKR", "FGQTL5", "GKRP", "glucokinase (hexokinase 4) regulator", "glucokinase regulator", "MLXIPL", "CHREBP", "MIO", "MONDOB", "WBSCR14", "WS-bHLH", "bHLHd14", "MLX interacting protein like", "MLX", "FTO", "ALKBH9", "GDFD", "BMIQ14", "fat mass and obesity associated", "FTO, alpha-ketoglutarate dependent dioxygenase", "ABCB11", "ABC16", "BRIC2", "BSEP", "PFIC-2", "PFIC2", "PGY4", "SPGP", "ATP binding cassette subfamily B member 11", "TFAP2B", "AP-2B", "AP2-B", "transcription factor AP-2 beta", "PDA2", "AP-2beta", "FADS1", "D5D", "FADS6", "FADSD5", "LLCDL1", "TU12", "fatty acid desaturase 1", "GIT2", "CAT-2", "CAT2", "PKL", "GIT ArfGAP 2", "HERPUD1", "HERP", "Mif1", "SUP", "homocysteine inducible ER protein with ubiquitin like domain 1", "TCF7L2", "TCF-4", "TCF4", "transcription factor 7 like 2"]}
-{"question": "Gene ITGA11 has a genetic association with diseases such as", "references": ["major depressive disorder", "recurrent depressive disorder", "major depression", "unipolar depression", "MDD", "clinical depression", "recurrent major depression", "single major depressive episode", "recurrent major depression in complete remission", "recurrent major depressive episodes, in full remission (disorder)", "major depression disorder", "depression", "attention deficit hyperactivity disorder", "ADHD", "hyperkinetic disorder", "attention deficit disorder", "AD/HD", "A.D.H.D", "attention deficit/hyperactivity disorder", "attention deficit hyperactivity syndrome", "Attention Deficit Disorder with Hyperactivity", "ADDH"]}
-{"question": "Gene WT4 has a genetic association with diseases such as", "references": ["nephroblastoma", "Wilms tumor", "adult nephroblastoma", "adult renal Wilms' tumor", "childhood renal Wilms' cancer", "renal Wilms tumor", "Wilms' tumor", "childhood renal Wilms tumor", "Wilms\u2019 tumour", "Wilm's tumour", "Wilm's tumor", "Wilms tumour"]}
-{"question": "Gene FCRL3 has a genetic association with diseases such as", "references": ["toxic diffuse goiter", "exophthalmic goiter", "Basedow's disease", "Graves' disease", "Grave's disease", "Graves disease", "multiple sclerosis", "MS", "encephalomyelitis disseminata", "insular sclerosis", "disseminated sclerosis", "generalized multiple sclerosis", "Generalized multiple sclerosis (disorder)", "generalised multiple sclerosis", "Multiple sclerosis; MS", "Multiple sclerosis", "type-1 diabetes", "IDDM", "insulin-dependent diabetes mellitus", "type I diabetes mellitus", "T1DM", "insulin dependent diabetes", "juvenile diabetes", "diabetes mellitus juvenile type", "DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM", "Diabetes Mellitus, Type 1", "Diabetes Mellitus, Insulin-Dependent, 1", "DIABETES MELLITUS, INSULIN-DEPENDENT", "Juvenile-Onset Diabetes", "Insulin-Dependent Diabetes Mellitus 1", "diabetes (type 1)", "type 1 diabetes mellitus"]}
-{"question": "Gene TRIM37 has a genetic association with diseases such as", "references": ["mulibrey nanism", "Muscle-Liver-Brain-Eye Nanism", "PERICARDIAL CONSTRICTION AND GROWTH FAILURE", "Perheentupa Syndrome", "MULIBREY NANISM", "MULIBREY dwarfism", "Pericardial constriction-growth failure syndrome"]}
-{"question": "Gene RHPN2 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "colorectal cancer", "colon cancer", "rectal cancer", "large intestine cancer", "Colorectal cancer, familial", "bowel cancer", "colon and rectal cancer"]}
-{"question": "Gene CDK6 has a genetic association with diseases such as", "references": ["rheumatoid arthritis", "Arthritis or polyarthritis, rheumatic", "atrophic Arthritis", "Rheumatoid arthritis with vasculitis", "Malignant rheumatoid arthritis", "Rheumatoid arthritis"]}
-{"question": "Gene Wolcott-Rallison syndrome has a genetic association with diseases such as", "references": ["EIF2AK3", "PEK", "PERK", "WRS", "eukaryotic translation initiation factor 2 alpha kinase 3"]}
-{"question": "Gene BOC has a genetic association with diseases such as", "references": ["dental caries", "dental caries extending into pulp", "dental caries of smooth surface", "dental caries pit and fissure", "tooth decay", "cavities", "caries"]}
-{"question": "Gene NR1H3 has a genetic association with diseases such as", "references": ["metabolic disease", "metabolic illness", "disorder of metabolic process", "metabolic disorder", "metabolic diseases", "disease of metabolism"]}
-{"question": "Gene EXOC4 has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene TYK2 has a genetic association with diseases such as", "references": ["rheumatoid arthritis", "Arthritis or polyarthritis, rheumatic", "atrophic Arthritis", "Rheumatoid arthritis with vasculitis", "Malignant rheumatoid arthritis", "Rheumatoid arthritis", "type-1 diabetes", "IDDM", "insulin-dependent diabetes mellitus", "type I diabetes mellitus", "T1DM", "insulin dependent diabetes", "juvenile diabetes", "diabetes mellitus juvenile type", "DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM", "Diabetes Mellitus, Type 1", "Diabetes Mellitus, Insulin-Dependent, 1", "DIABETES MELLITUS, INSULIN-DEPENDENT", "Juvenile-Onset Diabetes", "Insulin-Dependent Diabetes Mellitus 1", "diabetes (type 1)", "type 1 diabetes mellitus", "psoriasis"]}
-{"question": "Gene hypothyroidism has a genetic association with diseases such as", "references": ["MTF1", "MTF-1", "ZRF", "metal-regulatory transcription factor 1", "metal regulatory transcription factor 1", "PDE8B", "ADSD", "PPNAD3", "phosphodiesterase 8B", "VAV3", "vav guanine nucleotide exchange factor 3"]}
-{"question": "Gene GPC3 has a genetic association with diseases such as", "references": ["Simpson-Golabi-Behmel syndrome", "DGSX Golabi-Rosen syndrome", "Golabi-Rosen syndrome", "SGB syndrome", "Sara Angers syndrome", "Simpson dysmorphia syndrome", "X-linked dysplasia gigantism syndrome", "bulldog syndrome", "DGSX", "SGBS", "SGBS1", "Dysplasia Gigantism Syndrome, X-Linked", "SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1", "Simpson-Golabi-Behmel syndrome type 1", "SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1; SGBS1", "SDYS"]}
-{"question": "Gene MCM8 has a genetic association with diseases such as", "references": ["gestational hypertension", "hypertension induced by pregnancy", "pregnancy associated hypertension", "pregnancy toxemia", "Pregnancy-induced hypertension", "hypertension-associated pregnancy disorder", "Hypertension Associated Disorders of Pregnancy", "Hypertension-Associated Pregnancy Disorder", "pre-eclampsia", "Pre-eclampsia, preeclampsia", "Pre-eclampsia or eclampsia superimposed on pre-existing hypertension", "pregnancy associated hypertension", "preeclampsia/eclampsia", "toxaemia of pregnancy", "hypertension induced by pregnancy", "gestational hypertension", "proteinuric hypertension of pregnancy", "pregnancy toxemia", "pre-eclamptic toxaemia", "preeclampsia", "Pre-eclampsia"]}
-{"question": "Gene MYO10 has a genetic association with diseases such as", "references": ["major depressive disorder", "recurrent depressive disorder", "major depression", "unipolar depression", "MDD", "clinical depression", "recurrent major depression", "single major depressive episode", "recurrent major depression in complete remission", "recurrent major depressive episodes, in full remission (disorder)", "major depression disorder", "depression", "obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene pantothenate kinase-associated neurodegeneration has a genetic association with diseases such as", "references": ["PANK2", "C20orf48", "HARP", "HSS", "NBIA1", "PKAN", "pantothenate kinase 2"]}
-{"question": "Gene asthma has a genetic association with diseases such as", "references": ["ERBB4", "ALS19", "HER4", "p180erbB4", "erb-b2 receptor tyrosine kinase 4", "RAP1GAP2", "GARNL4", "RAP1GA3", "RAP1 GTPase activating protein 2", "FBXL7", "FBL6", "FBL7", "F-box and leucine-rich repeat protein 7", "F-box and leucine rich repeat protein 7", "CDHR3", "CDH28", "cadherin related family member 3", "GSDMB", "GSDML", "PRO2521", "PP4052", "gasdermin B", "GSDMB-1", "IL33", "C9orf26", "DVS27", "IL1F11", "NF-HEV", "NFEHEV", "Interleukin 33", "IL-33", "IL-1F11", "RAD50", "NBSLD", "RAD502", "hRad50", "Rad50", "RAD50 double strand break repair protein", "GSDMA", "GSDM", "GSDM1", "FKSG9", "gasdermin A", "IL13", "IL-13", "P600", "interleukin 13", "IGSF3", "EWI-3", "V8", "LCDD", "immunoglobulin superfamily member 3", "HPSE2", "HPA2", "HPR2", "UFS", "UFS1", "heparanase 2 (inactive)", "PSAP", "GLBA", "SAP1", "prosaposin", "SAP2", "PSAPD", "PARK24", "ATG3", "ATG3", "APG3", "APG3-LIKE", "APG3L", "PC3-96", "autophagy related 3", "MKLN1", "TWA2", "muskelin 1", "XPR1", "SYG1", "X3", "IBGC6", "xenotropic and polytropic retrovirus receptor 1", "SLC53A1", "ABI3BP", "NESHBP", "TARSH", "ABI family member 3 binding protein", "HLA-DQA1", "CD", "CELIAC1", "DQ-A1", "GSE", "HLA-DQA", "Major histocompatibility complex, class II, DQ alpha 1", "DQA1", "ACO1", "ACONS", "HEL60", "IREB1", "IREBP", "IREBP1", "IRP1", "aconitase 1", "ZNF665", "ZFP160L", "zinc finger protein 665", "PRKG1", "AAT8", "PKG", "PRKG1B", "PRKGR1B", "cGK", "cGK 1", "cGK1", "cGKI", "cGKI-BETA", "cGKI-alpha", "protein kinase, cGMP-dependent, type I", "PKG1", "protein kinase cGMP-dependent 1", "IL6R", "CD126", "IL-6R-1", "IL-6RA", "IL6Q", "IL6RA", "IL6RQ", "gp80", "Interleukin-6 receptor", "interleukin 6 receptor", "GAB1", "GRB2 associated binding protein 1", "DFNB26", "PBX2", "G17", "HOX12", "PBX2MHC", "PBX homeobox 2", "NOTCH4", "INT3", "notch 4", "notch receptor 4", "TSBP1", "TSBP", "chromosome 6 open reading frame 10", "testis expressed basic protein 1", "C6orf10", "IKZF4", "EOS", "ZNFN1A4", "IKAROS family zinc finger 4", "IL1RL1", "DER4", "FIT-1", "IL33R", "ST2", "ST2L", "ST2V", "T1", "interleukin 1 receptor like 1", "SLC30A8", "ZNT8", "ZnT-8", "solute carrier family 30 member 8", "IL18R1", "CD218a", "CDw218a", "IL-1Rrp", "IL18RA", "IL1RRP", "interleukin 18 receptor 1", "IL-18R-alpha", "IL18Ralpha2", "IL-18Ralpha", "SMAD3", "HSPC193", "HsT17436", "JV15-2", "LDS1C", "LDS3", "MADH3", "SMAD family member 3", "IL2RB", "CD122", "IL15RB", "P70-75", "interleukin 2 receptor subunit beta", "IMD63", "SLC22A5", "CDSP", "OCTN2", "solute carrier family 22 member 5", "RORA", "NR1F1", "ROR1", "ROR2", "ROR3", "RZR-ALPHA", "RZRA", "RAR related orphan receptor A", "IDDECA", "PDE4D", "ACRDYS2", "DPDE3", "HSPDE4D", "PDE43", "PDE4DN2", "STRK1", "phosphodiesterase 4D"]}
-{"question": "Gene clubfoot has a genetic association with diseases such as", "references": ["PITX1", "BFT", "CCF", "LBNBG", "POTX", "PTX1", "paired like homeodomain 1"]}
-{"question": "Gene SLC34A2 has a genetic association with diseases such as", "references": ["pulmonary alveolar microlithiasis", "pulmonary alveolar microlithiasis (disorder)", "Pulmonary alveolar microlithiasis"]}
-{"question": "Gene Larsen syndrome has a genetic association with diseases such as", "references": ["FLNB", "ABP-278", "ABP-280", "AOI", "FH1", "FLN-B", "FLN1L", "LRS1", "SCT", "TABP", "TAP", "filamin B"]}
-{"question": "Gene LMNB2 has a genetic association with diseases such as", "references": ["Barraquer\u2013Simons syndrome", "Lipodystrophy, Partial, Progressive", "Barraquer-Simons syndrome", "Apld, Susceptibility to", "susceptibility to partial acquired lipodystrophy", "LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO", "Partial Acquired Lipodystrophy", "Progressive cephalothoracic lipodystrophy", "APLD", "Lipodystrophy, Cephalothoracic Type", "LIPODYSTROPHY, PARTIAL, ACQUIRED, SUSCEPTIBILITY TO; APLD"]}
-{"question": "Gene breast cancer has a genetic association with diseases such as", "references": ["MAP3K1", "MAPKKK1", "MEKK", "MEKK 1", "MEKK1", "SRXY6", "mitogen-activated protein kinase kinase kinase 1", "FGFR2", "BBDS", "BEK", "BFR-1", "CD332", "CEK3", "CFD1", "ECT1", "JWS", "K-SAM", "KGFR", "TK14", "TK25", "fibroblast growth factor receptor 2", "MDM4", "HDMX", "MDMX", "MRP1", "MDM4, p53 regulator", "MDM4 regulator of p53", "BMFS6", "TERT", "CMM9", "DKCA2", "DKCB4", "EST2", "PFBMFT1", "TCS1", "TP2", "TRT", "hEST2", "hTRT", "telomerase reverse transcriptase", "HTERT", "PLCG2", "APLAID", "FCAS3", "PLC-IV", "PLC-gamma-2", "phospholipase C gamma 2", "ZNF365", "Su48", "UAN", "ZNF365D", "zinc finger protein 365", "PEX14", "NAPP2", "PBD13A", "Pex14p", "dJ734G22.2", "peroxisomal biogenesis factor 14", "EBF1", "COE1", "EBF", "O/E-1", "OLF1", "early B-cell factor 1", "early B cell factor 1", "EBF transcription factor 1", "MRTFA", "BSAC", "MAL", "MRTF-A", "megakaryoblastic leukemia (translocation) 1", "MKL", "MKL1", "myocardin related transcription factor A", "TGFBR2", "AAT3", "FAA3", "LDS1B", "LDS2", "LDS2B", "MFS2", "RIIC", "TAAD2", "TGFR-2", "TGFbeta-RII", "transforming growth factor beta receptor 2", "TBR-ii", "TBRII", "TET2", "KIAA1546", "MDS", "tet methylcytosine dioxygenase 2", "Tet methylcytosine dioxygenase 2", "IMD75", "TCF7L2", "TCF-4", "TCF4", "transcription factor 7 like 2", "CCDC88C", "DAPLE", "HKRP2", "KIAA1509", "SCA40", "coiled-coil domain containing 88C", "HYC1", "CDYL2", "PCCP1", "chromodomain protein, Y-like 2", "chromodomain Y like 2", "SLC4A7", "NBC2", "NBC3", "NBCN1", "SBC2", "SLC4A6", "solute carrier family 4 member 7", "ZMIZ1", "MIZ", "RAI17", "TRAFIP10", "ZIMP10", "hZIMP10", "zinc finger MIZ-type containing 1", "NEDDFSA", "PDE4D", "ACRDYS2", "DPDE3", "HSPDE4D", "PDE43", "PDE4DN2", "STRK1", "phosphodiesterase 4D", "NTN1", "NTN1L", "netrin 1", "MRMV4", "SYT6", "sytVI", "synaptotagmin 6", "PBX1", "PBX homeobox 1", "CAKUHED", "SIAH2", "hSiah2", "siah E3 ubiquitin protein ligase 2", "ERBB4", "ALS19", "HER4", "p180erbB4", "erb-b2 receptor tyrosine kinase 4", "ESR1", "ER", "ESR", "ESRA", "ESTRR", "Era", "NR3A1", "estrogen receptor 1", "ZNF577", "zinc finger protein 577", "ABCC4", "MOAT-B", "MOATB", "MRP4", "ATP binding cassette subfamily C member 4", "GRIK1", "EAA3", "EEA3", "GLR5", "GLUR5", "GluK1", "gluR-5", "glutamate ionotropic receptor kainate type subunit 1", "FBN1", "ACMICD", "ECTOL1", "FBN", "GPHYSD2", "MASS", "MFS1", "OCTD", "SGS", "SSKS", "WMS", "WMS2", "MFLS", "fibrillin 1", "AKT1", "AKT", "CWS6", "PKB", "PKB-ALPHA", "PRKBA", "RAC", "RAC-ALPHA", "AKT serine/threonine kinase 1"]}
-{"question": "Gene NTRK3 has a genetic association with diseases such as", "references": ["Gaucher's disease", "Gaucher disease", "acid beta-glucosidase deficiency", "glocucerebrosidase deficiency", "glucosylceramide beta-glucosidase deficiency", "kerasin thesaurismosis", "lipoid histiocytosis (kerasin type)", "lipoid histiocytosis", "Glucocerebrosidase deficiency"]}
-{"question": "Gene kidney disease has a genetic association with diseases such as", "references": ["SLC13A3", "NADC3", "SDCT2", "solute carrier family 13 member 3", "ARLIAK", "TFDP2", "DP2", "transcription factor Dp-2", "PRKAG2", "AAKG", "AAKG2", "CMH6", "H91620p", "WPWS", "protein kinase AMP-activated non-catalytic subunit gamma 2", "DACH1", "DACH", "dachshund family transcription factor 1", "SLC22A2", "OCT2", "solute carrier family 22 member 2", "WDR37", "WD repeat domain 37", "NOCGUS", "WDR72", "AI2A3", "WD repeat domain 72", "SHROOM3", "APXL3", "SHRM", "ShrmL", "MSTP013", "shroom family member 3", "PVT1", "LINC00079", "NCRNA00079", "onco-lncRNA-100", "Pvt1 oncogene (non-protein coding)", "MYC", "MIR1204HG", "Pvt1 oncogene"]}
-{"question": "Gene Warfarin resistance has a genetic association with diseases such as", "references": ["CYP2A6", "CPA6", "CYP2A", "CYP2A3", "CYPIIA6", "P450C2A", "P450PB", "cytochrome P450 family 2 subfamily A member 6"]}
-{"question": "Gene AP2A2 has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene TCF7L2 has a genetic association with diseases such as", "references": ["type 2 diabetes", "NIDDM", "non-insulin-dependent diabetes mellitus", "type II diabetes mellitus", "Diabetes mellitus type 2", "Rare insulin-independent diabetes mellitus", "Diabetes Mellitus, Type 2", "type 2 diabetes mellitus", "diabetes (type 2)", "bipolar disorder", "BP", "manic depression", "BPAD", "breast cancer", "malignant neoplasm of breast", "malignant tumor of the breast", "mammary cancer", "primary breast cancer", "breast disorder", "coronary artery disease", "CAD", "atherosclerotic heart disease", "coronary heart disease", "ischemic heart disease", "IHD", "atherosclerotic cardiovascular disease", "CHD (coronary heart disease)", "coronary arteriosclerosis", "CHD", "coronary artery arteriosclerosis (disease)", "atherosclerosis of coronary artery", "Coronary Atherosclerosis", "metabolic disease", "metabolic illness", "disorder of metabolic process", "metabolic disorder", "metabolic diseases", "disease of metabolism", "colorectal cancer", "colon cancer", "rectal cancer", "large intestine cancer", "Colorectal cancer, familial", "bowel cancer", "colon and rectal cancer"]}
-{"question": "Gene Parastremmatic dwarfism has a genetic association with diseases such as", "references": ["TRPV4", "BCYM3", "CMT2C", "HMSN2C", "OTRPC4", "SMAL", "SPSMA", "SSQTL1", "TRP12", "VRL2", "VROAC", "transient receptor potential cation channel subfamily V member 4"]}
-{"question": "Gene coloboma has a genetic association with diseases such as", "references": ["PAX6", "AN", "AN2", "D11S812E", "FVH1", "MGDA", "WAGR", "paired box 6", "ASGD5", "SALL2", "COLB", "HSAL2", "Sal-2", "ZNF795", "p150(Sal2)", "spalt-like transcription factor 2", "spalt like transcription factor 2"]}
-{"question": "Gene LIN28B has a genetic association with diseases such as", "references": ["neuroblastoma", "NB", "neuroblastoma (Schwannian Stroma-Poor)"]}
-{"question": "Gene trichothiodystrophy syndromes has a genetic association with diseases such as", "references": ["GTF2E2", "FE", "TF2E2", "TFIIE-B", "TTD6", "general transcription factor IIE subunit 2", "RNF113A", "Cwc24", "RNF113", "ZNF183", "TTD5", "ring finger protein 113A", "GTF2H5", "C6orf175", "TFB5", "TFIIH", "TGF2H5", "TTD", "TTD-A", "TTDA", "bA120J8.2", "TTD3", "general transcription factor IIH subunit 5", "MPLKIP", "ABHS", "C7orf11", "ORF20", "TTD4", "M-phase specific PLK1 interacting protein"]}
-{"question": "Gene Carney complex has a genetic association with diseases such as", "references": ["PRKAR1A", "ACRDYS1", "ADOHR", "CAR", "CNC", "CNC1", "PKR1", "PPNAD1", "PRKAR1", "TSE1", "protein kinase cAMP-dependent type I regulatory subunit alpha", "MYH8", "MyHC-peri", "MyHC-pn", "gtMHC-F", "DA7", "myosin, heavy chain 8, skeletal muscle, perinatal", "myosin heavy chain 8"]}
-{"question": "Gene CLEC7A has a genetic association with diseases such as", "references": ["chronic mucocutaneous candidiasis", "chronic Mucocutaneous Candidiasis", "Candidiasis, Familial Chronic Mucocutaneous", "CANDIDIASIS, FAMILIAL, 4", "CANDF4", "Candidiasis, Familial, type 4", "CANDIDIASIS, FAMILIAL, 4; CANDF4"]}
-{"question": "Gene ALPK1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "leukopenia", "leucopenia", "leukocytopenia"]}
-{"question": "Gene adrenocorticotropic hormone deficiency has a genetic association with diseases such as", "references": ["TBX19", "TBS19", "TPIT", "dJ747L4.1", "T-box 19", "T-box transcription factor 19"]}
-{"question": "Gene NMNAT2 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene PDE1C has a genetic association with diseases such as", "references": ["endometriosis"]}
-{"question": "Gene PLD5 has a genetic association with diseases such as", "references": ["coronary artery disease", "CAD", "atherosclerotic heart disease", "coronary heart disease", "ischemic heart disease", "IHD", "atherosclerotic cardiovascular disease", "CHD (coronary heart disease)", "coronary arteriosclerosis", "CHD", "coronary artery arteriosclerosis (disease)", "atherosclerosis of coronary artery", "Coronary Atherosclerosis"]}
-{"question": "Gene Schinzel\u2013Giedion syndrome has a genetic association with diseases such as", "references": ["SETBP1", "SET binding protein 1", "SEB", "MRD29", "SET bindign protein 1"]}
-{"question": "Gene ACAT1 has a genetic association with diseases such as", "references": ["beta-ketothiolase deficiency", "2-methyl-3-hydroxybutyricacidemia", "3-ketothiolase deficiency", "3-oxothiolase deficiency", "Mitochondrial acetoacetyl-CoA Thiolase deficiency", "alpha-methylacetoaceticaciduria", "peroxisomal thiolase deficiency (disorder)", "peroxisomal thiolase deficiency", "BKT", "Beta-Ketothiolase Deficiency", "T2 Deficiency", "3-Ktd Deficiency", "Alpha-methyl-acetoacetyl-CoA thiolase deficiency", "Mitochondrial acetoacetyl-coenzyme A thiolase deficiency", "ALPHA-METHYLACETOACETIC ACIDURIA", "2-Methyl-3-Hydroxybutyric Acidemia", "Mat Deficiency", "Alpha methylacetoacetic aciduria"]}
-{"question": "Gene phaeochromocytoma has a genetic association with diseases such as", "references": ["SDHB", "CWS2", "IP", "PGL4", "SDH", "SDH1", "SDH2", "SDHIP", "succinate dehydrogenase complex iron sulfur subunit B", "MC2DN4", "TMEM127", "transmembrane protein 127", "SDHD", "CBT1", "CII-4", "CWS3", "PGL", "PGL1", "QPs3", "SDH4", "cybS", "succinate dehydrogenase complex subunit D", "MC2DN3", "GDNF", "ATF1", "ATF2", "HFB1-GDNF", "HSCR3", "glial cell derived neurotrophic factor", "ATF", "MAX", "bHLHd4", "max", "MYC associated factor X"]}
-{"question": "Gene PRKAR2B has a genetic association with diseases such as", "references": ["bladder cancer", "tumor of the bladder", "Malignant Tumor of Urinary Bladder", "Malignant Neoplasm, Urinary Bladder", "Malignant Urinary Bladder Tumor", "Malignant Tumor of Bladder", "cancer of urinary bladder", "Malignant Bladder Tumor", "Urinary Bladder Malignant Tumor", "Malignant Tumor, Urinary Bladder", "Malignant Tumor of the Bladder", "Malignant Bladder Neoplasm", "Malignant Urinary Bladder Neoplasm", "Malignant Neoplasm of the Urinary Bladder", "Malignant Neoplasm of Urinary Bladder", "Malignant Neoplasm of Bladder", "Malignant Neoplasm of the Bladder", "Urinary Bladder Malignant Neoplasm", "Malignant Tumor of the Urinary Bladder", "Malignant Neoplasm, Bladder", "urinary bladder cancer"]}
-{"question": "Gene Fraser syndrome has a genetic association with diseases such as", "references": ["FRAS1", "Fraser extracellular matrix complex subunit 1", "FRASRS1"]}
-{"question": "Gene ATF1 has a genetic association with diseases such as", "references": ["Angiomatoid fibrous histiocytoma", "histiocytoma, Angiomatoid fibrous", "HISTIOCYTOMA, ANGIOMATOID FIBROUS", "AFH", "Angiomatoid Fibrous Histiocytoma", "Angiomatoid Malignant Fibrous Histiocytoma"]}
-{"question": "Gene Vibratory angioedema has a genetic association with diseases such as", "references": ["ADGRE2", "CD312", "VBU", "EMR2", "adhesion G protein-coupled receptor E2", "CD97"]}
-{"question": "Gene prolidase deficiency has a genetic association with diseases such as", "references": ["PEPD", "PROLIDASE", "peptidase D"]}
-{"question": "Gene TRPS1 has a genetic association with diseases such as", "references": ["major depressive disorder", "recurrent depressive disorder", "major depression", "unipolar depression", "MDD", "clinical depression", "recurrent major depression", "single major depressive episode", "recurrent major depression in complete remission", "recurrent major depressive episodes, in full remission (disorder)", "major depression disorder", "depression", "trichorhinophalangeal syndrome type II", "Langer-Giedion syndrome", "Trichorhinophalangeal dysplasia type II", "TRPS2", "TRICHORHINOPHALANGEAL SYNDROME, TYPE II; TRPS2", "Deletion 8q24.1", "Trichorhinophalangeal syndrome type 2", "TRICHORHINOPHALANGEAL SYNDROME, TYPE II", "Monosomy 8q24.1", "Chromosome 8Q24.1 Deletion Syndrome"]}
-{"question": "Gene MAP3K8 has a genetic association with diseases such as", "references": ["inflammatory bowel diseases", "IBD", "inflammatory bowel disease"]}
-{"question": "Gene ATXN3 has a genetic association with diseases such as", "references": ["coronary artery disease", "CAD", "atherosclerotic heart disease", "coronary heart disease", "ischemic heart disease", "IHD", "atherosclerotic cardiovascular disease", "CHD (coronary heart disease)", "coronary arteriosclerosis", "CHD", "coronary artery arteriosclerosis (disease)", "atherosclerosis of coronary artery", "Coronary Atherosclerosis", "cleft lip and cleft palate", "cleft palate", "cleft lip", "cheilopalatoschisis", "Complete unilateral cleft palate with cleft lip (disorder)", "Unilateral complete cleft palate with cleft lip", "Unilateral complete cleft palate with cleft lip (disorder)", "Unilateral incomplete cleft palate with cleft lip", "Unilateral incomplete cleft palate with cleft lip (disorder)", "cleft palate with cleft lip, unilateral, complete", "cleft palate with cleft lip, unilateral, incomplete", "incomplete unilateral cleft palate with cleft lip (disorder)", "orofacial cleft", "obsolete cheilopalatoschisis", "Machado-Joseph disease", "Azorean disease (disorder)", "MJD", "spinocerebellar ataxia type 3", "spinocerebellar ataxia 3", "Azorean disease", "Nigrospinodentatal Degeneration", "MACHADO-JOSEPH DISEASE; MJD", "Autosomal dominant striatonigral degeneration", "Nigro-spino-dentatal degeneration with nuclear ophthalmoplegia", "Spinopontine Atrophy", "Spinocerebellar Atrophy 3", "Machado disease", "Azorean Neurologic Disease", "Azorean disease of the nervous system", "SCA3", "MACHADO-JOSEPH DISEASE"]}
-{"question": "Gene XYLT2 has a genetic association with diseases such as", "references": ["Spondylo-ocular syndrome", "SPONDYLOOCULAR SYNDROME", "SPONDYLOOCULAR SYNDROME; SOS", "SOS", "inherited pseudoxanthoma elasticum", "Gronblad-Strandberg syndrome", "Pseudoxanthoma elasticum, PXE", "PSEUDOXANTHOMA ELASTICUM; PXE", "Pseudoxanthoma Elasticum, Modifier of Severity of", "Pxe, Modifier of Severity of", "PSEUDOXANTHOMA ELASTICUM", "Gronblad-Strandberg-Touraine syndrome", "PXE", "Gronblad Strandberg syndrome"]}
-{"question": "Gene tuberculosis has a genetic association with diseases such as", "references": ["DSCAM", "CHD2", "CHD2-42", "CHD2-52", "DSCAM", "DS cell adhesion molecule", "DYNC2H1", "ATD3", "DHC1b", "DHC2", "DNCH2", "DYH1B", "SRPS2B", "SRTD3", "hdhc11", "dynein cytoplasmic 2 heavy chain 1", "IL2RB", "CD122", "IL15RB", "P70-75", "interleukin 2 receptor subunit beta", "IMD63", "ZFPM2", "DIH3", "FOG2", "ZC2HC11B", "ZNF89B", "hFOG-2", "SRXY9", "zinc finger protein, FOG family member 2", "SPON1", "VSGP/F-spondin", "f-spondin", "Spondin 1"]}
-{"question": "Gene FAM135B has a genetic association with diseases such as", "references": ["periodontitis", "pyorrhea", "chronic pericementitis", "periodontium inflammation", "periodontiumitis"]}
-{"question": "Gene ARL15 has a genetic association with diseases such as", "references": ["type 2 diabetes", "NIDDM", "non-insulin-dependent diabetes mellitus", "type II diabetes mellitus", "Diabetes mellitus type 2", "Rare insulin-independent diabetes mellitus", "Diabetes Mellitus, Type 2", "type 2 diabetes mellitus", "diabetes (type 2)", "rheumatoid arthritis", "Arthritis or polyarthritis, rheumatic", "atrophic Arthritis", "Rheumatoid arthritis with vasculitis", "Malignant rheumatoid arthritis", "Rheumatoid arthritis", "alcohol dependence", "alcoholism", "alcohol dependence syndrome", "alcohol addiction"]}
-{"question": "Gene Nance-Horan syndrome has a genetic association with diseases such as", "references": ["NHS", "CTRCT40", "CXN", "SCML1", "NHS actin remodeling regulator"]}
-{"question": "Gene SPRTN has a genetic association with diseases such as", "references": ["progeroid features-hepatocellular carcinoma predisposition syndrome", "RJALS", "Ruijs-Aalfs syndrome", "progeroid features-hepatocellular carcinoma predisposition syndrome"]}
-{"question": "Gene DSTYK has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "hereditary spastic paraplegia 23", "spastic paraplegia type 23", "Lison syndrome", "SPG23", "spastic paraplegia with pigmentary abnormalities", "Spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome", "spastic paraplegia 23", "SPASTIC PARAPLEGIA 23; SPG23", "Autosomal recessive spastic paraplegia type 23", "Spastic Paraparesis, Vitiligo, Premature Graying, Characteristic Facies", "hereditary spastic paraplegia type 23"]}
-{"question": "Gene KRT5 has a genetic association with diseases such as", "references": ["basal-cell carcinoma", "Polypoid basal cell carcinoma", "Nodular basal cell carcinoma", "basal cell carcinoma", "BASAL CELL carcinoma OF SKIN", "Basal cell cancer", "Basal cell carcinoma NOS (morphologic abnormality)", "Basal cell carcinoma of skin (disorder)", "Basal cell neoplasm (morphologic abnormality)", "Basal cell neoplasm NOS (morphologic abnormality)", "Basal cell tumor", "Basal cell tumor (morphologic abnormality)", "Epithelioma basal cell (disorder)", "Rodent ulcer", "malignant Basal cell neoplasm", "malignant basal cell tumor", "malignant basal cell tumor (morphologic abnormality)", "BCC", "Basal cell neoplasm", "Epithelioma basal cell", "Basal Cell Skin Carcinoma", "Basal Cell Carcinoma of the Skin", "Skin Basal Cell Carcinoma", "Basal Cell Epithelioma", "Skin Basal Cell Cancer", "epidermolysis bullosa herpetiformis", "epidermolysis bullosa simplex Dowling-Meara type", "EBS-gen sev", "EBSDM", "epidermolysis bullosa herpetiformis Dowling-Meara type", "epidermolysis bullosa simplex, herpetiformis", "generalized severe epidermolysis bullosa simplex", "Epidermolysis Bullosa Simplex, Generalized Severe", "EPIDERMOLYSIS BULLOSA SIMPLEX, DOWLING-MEARA TYPE; EBSDM", "Dowling-Meara type epidermolysis bullosa simplex", "EBS-DM", "EPIDERMOLYSIS BULLOSA SIMPLEX, DOWLING-MEARA TYPE", "Epidermolysis Bullosa Herpetiformis, Dowling-Meara Type", "Localized epidermolysis bullosa simplex", "Weber-Cockayne epidermolysis bullosa simplex", "Epidermolysis bullosa simplex, Weber-Cockayne type", "Weber-Cockayne syndrome", "Ebs, Acral Form", "Epidermolysis Bullosa of Hands and Feet", "Weber-Cockayne type epidermolysis bullosa simplex", "Epidermolysis bullosa simplex of palms and soles", "EBS-loc", "EPIDERMOLYSIS BULLOSA SIMPLEX, LOCALIZED", "epidermolysis bullosa simplex localized type", "epidermolysis bullosa simplex Weber-Cockayne type", "Generalized epidermolysis bullosa simplex", "Koebner variant of generalized epidermolysis bullosa simplex", "Generalized EBS, non-Dowling-Meara type", "EPIDERMOLYSIS BULLOSA SIMPLEX, GENERALIZED", "Epidermolysis bullosa simplex, K\u00f6bner type", "Epidermolysis bullosa simplex, Koebner type", "Epidermolysis bullosa simplex, KC6bner type", "Ebs, Generalized", "epidermolysis bullosa simplex generalized type", "epidermolysis bullosa simplex Koebner type", "Dowling-Degos disease", "dark dot disease", "reticular pigment anomaly of flexures", "DDD1", "DOWLING-DEGOS DISEASE 1; DDD1", "Ddd"]}
-{"question": "Gene Alpha-thalassemia mental retardation syndrome has a genetic association with diseases such as", "references": ["ATRX", "ATR2", "JMS", "MRXHF1", "RAD54", "RAD54L", "SFM1", "SHS", "XH2", "XNP", "ZNF-HX", "MRX52", "alpha thalassemia/mental retardation syndrome X-linked", "ATRX, chromatin remodeler", "ATRX chromatin remodeler"]}
-{"question": "Gene KCNJ10 has a genetic association with diseases such as", "references": ["EAST syndrome", "SeSAME syndrome", "epilepsy, ataxia, sensorineural deafness and tubulopathy", "seizures, sensorineural deafness, ataxia, mental retardation and electrolyte imbalance", "SESAMES", "Epilepsy, Ataxia, Sensorineural Deafness, and Tubulopathy", "SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE; SESAMES", "East Syndrome", "Seizures-sensorineural deafness-ataxia-intellectual disability-electrolyte imbalance syndrome", "SEIZURES, SENSORINEURAL DEAFNESS, ATAXIA, MENTAL RETARDATION, AND ELECTROLYTE IMBALANCE"]}
-{"question": "Gene Howel\u2013Evans syndrome has a genetic association with diseases such as", "references": ["RHBDF2", "RHBDL5", "RHBDL6", "TOC", "TOCG", "TEC", "iRhom2", "rhomboid 5 homolog 2"]}
-{"question": "Gene AATK has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene HR has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "Atrichia with papular lesions", "atrichia with papular lesions", "APL", "papular atrichia", "ATRICHIA WITH PAPULAR LESIONS; APL"]}
-{"question": "Gene Duane-radial ray syndrome has a genetic association with diseases such as", "references": ["SALL4", "DRRS", "HSAL4", "ZNF797", "dJ1112F19.1", "spalt-like transcription factor 4", "spalt like transcription factor 4", "IVIC"]}
-{"question": "Gene ESRRB has a genetic association with diseases such as", "references": ["nonsyndromic deafness", "nonsyndromic hearing loss", "nonsyndromic hereditary hearing loss", "Familial deafness", "Non-syndromic genetic deafness", "Isolated genetic deafness"]}
-{"question": "Gene PDLIM5 has a genetic association with diseases such as", "references": ["prostate cancer", "malignant tumor of the prostate", "prostatic cancer", "tumor of the prostate", "malignant neoplasm of the prostate", "prostate cancer, familial", "hereditary prostate cancer"]}
-{"question": "Gene FARP2 has a genetic association with diseases such as", "references": ["chronic lymphocytic leukemia", "B-cell chronic lymphocytic leukemia", "CLL", "chronic lymphatic leukemia", "lymphoplasmacytic leukemia", "B-cell chronic lymphoid leukemia", "B-Cell Chronic Lymphogenous Leukemia", "Chronic Lymphocytic Leukemia (CLL)", "Hematopoeitic - Chronic Lymphocytic Leukemia (CLL)", "Chronic B-Cell Lymphocytic Leukemia", "B-Cell CLL", "Leukemia, Chronic Lymphatic", "B Cell CLL", "Small lymphocytic lymphoma", "BCLL", "LEUKEMIA, CHRONIC LYMPHOCYTIC; CLL", "B Cell Chronic Lymphocytic Leukemia", "B-CLL", "Chronic Lymphocytic Leukemia", "B Cell Lymphocytic Leukemia", "Chronic Lymphogenous Leukemia", "B-Cell Lymphocytic Leukemia", "LEUKEMIA, CHRONIC LYMPHOCYTIC", "Chronic lymphocytic leukemia, NOS", "Chronic lymphocytic leukemia; CLL", "Leukemia, Lymphocytic, Chronic, B-Cell", "Chronic lymphocytic leukaemia", "chronic lymphocytic leukaemia"]}
-{"question": "Gene SRL has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene EPHA6 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene SH2B1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene GABRB1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene dermatofibrosarcoma protuberans has a genetic association with diseases such as", "references": ["PDGFB", "IBGC5", "PDGF-2", "PDGF2", "SIS", "SSV", "c-sis", "platelet derived growth factor subunit B"]}
-{"question": "Gene IL33 has a genetic association with diseases such as", "references": ["asthma", "exercise-induced asthma", "chronic obstructive asthma", "chronic obstructive asthma with status asthmaticus", "chronic obstructive asthma with acute exacerbation", "bronchial hyperreactivity", "Exercise induced asthma", "Asthma", "asthma brionchiole", "endometriosis"]}
-{"question": "Gene Duane retraction syndrome has a genetic association with diseases such as", "references": ["CHN1", "chimerin 1", "ARHGAP2", "CHN", "DURS2", "NC", "RHOGAP2"]}
-{"question": "Gene Gitelman syndrome has a genetic association with diseases such as", "references": ["SLC12A3", "NCC", "NCCT", "TSC", "solute carrier family 12 member 3", "Sodium-chloride symporter"]}
-{"question": "Gene dermatochalasis has a genetic association with diseases such as", "references": ["ATP6V0A2", "A2", "ARCL", "ARCL2A", "ATP6A2", "ATP6N1D", "J6B7", "RTF", "STV1", "TJ6", "TJ6M", "TJ6S", "VPH1", "WSS", "ATPase H+ transporting V0 subunit a2"]}
-{"question": "Gene RAD21 has a genetic association with diseases such as", "references": ["Mungan syndrome", "Pseudoobstruction, Chronic Idiopathic Intestinal, With Barrett Esophagus and Cardiac Abnormalities", "Visceral Neuromyopathy, Familial, With Pseudoobstruction, Megaduodenum, Barrett Esophagus, and Cardiac Abnormalities", "MUNGAN SYNDROME", "MUNGAN SYNDROME; MGS", "Cornelia de Lange syndrome", "Brachmann de Lange syndrome", "De Lange syndrome", "Brachmann-de Lange syndrome", "CdLS", "Cornelia de Lange syndrome", "Brachmann de Lange syndrome", "De Lange syndrome", "Brachmann-de Lange syndrome", "CdLS", "sclerocornea", "isolated congenital sclerocornea", "Mungan syndrome", "Pseudoobstruction, Chronic Idiopathic Intestinal, With Barrett Esophagus and Cardiac Abnormalities", "Visceral Neuromyopathy, Familial, With Pseudoobstruction, Megaduodenum, Barrett Esophagus, and Cardiac Abnormalities", "MUNGAN SYNDROME", "MUNGAN SYNDROME; MGS", "acute myeloid leukemia", "AML - acute Myeloid Leukemia", "Leukemia, Myelocytic, acute", "acute myeloblastic leukemia", "acute myelogenous leukemia", "Acute myelogenous leukemia; AML", "Acute Granulocytic Leukemia", "LEUKEMIA, ACUTE MYELOID; AML", "Acute non lymphoblastic leukemia", "myeloid leukemia, acute", "LEUKEMIA, ACUTE MYELOID", "ANLL", "Hematopoeitic - Acute Myleogenous Leukemia (AML)", "Acute Myeloid Leukemia", "Leukemia, Acute Myeloid, Susceptibility to", "Acute Myeloid Leukemia (AML)", "Leukemia, Acute Myelogenous", "Acute Myelogenous Leukemias", "AML", "Acute Nonlymphocytic Leukemia", "Acute Myelocytic Leukemia", "acute myeloid leukaemia"]}
-{"question": "Gene RASGRF2 has a genetic association with diseases such as", "references": ["eating disorder", "ED", "feeding and eating disorders", "feeding disorder", "eating disorders", "cleft lip and cleft palate", "cleft palate", "cleft lip", "cheilopalatoschisis", "Complete unilateral cleft palate with cleft lip (disorder)", "Unilateral complete cleft palate with cleft lip", "Unilateral complete cleft palate with cleft lip (disorder)", "Unilateral incomplete cleft palate with cleft lip", "Unilateral incomplete cleft palate with cleft lip (disorder)", "cleft palate with cleft lip, unilateral, complete", "cleft palate with cleft lip, unilateral, incomplete", "incomplete unilateral cleft palate with cleft lip (disorder)", "orofacial cleft", "obsolete cheilopalatoschisis"]}
-{"question": "Gene Keratitis\u2013ichthyosis\u2013deafness syndrome has a genetic association with diseases such as", "references": ["GJB2", "CX26", "DFNA3", "DFNA3A", "DFNB1", "DFNB1A", "HID", "KID", "NSRD1", "PPK", "gap junction protein beta 2", "BAPS"]}
-{"question": "Gene DYNC1I1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "smallpox", "ordinary smallpox", "variola", "variola vera"]}
-{"question": "Gene JAK2 has a genetic association with diseases such as", "references": ["Crohn's disease", "regional enteritis", "Crohn disease", "Crohn's disease of colon (disorder)", "Crohn's disease of large bowel", "Granulomatous Colitis", "regional Ileitis", "regional colitis", "regional enteritis of small intestine with large intestine", "regional enteritis of the large bowel", "regional ileocolitis", "Crohn's disease of colon", "Crohn", "polycythemia vera", "Osler-Vaquez syndrome", "PV", "erythremia (morphologic abnormality)", "polycythaemia rubra vera", "proliferative polycythaemia", "Polycythemia Rubra Vera", "POLYCYTHEMIA VERA; PV", "Vaquez disease", "Polycythemia vera", "Osler-Vaquez disease", "Acquired primary erythrocytosis", "myelofibrosis", "Cutaneous myelofibrosis", "Agnogenic myeloid metaplasia", "Aleukemic myelosis", "Megakaryocytic myelosclerosis", "bone Marrow Fibrosis", "myelosclerosis", "primary myelofibrosis", "Idiopathic Bone Marrow Fibrosis", "Osteomyelofibrosis", "chronic idiopathic myelofibrosis", "Myelofibrosis with myeloid metaplasia", "MYELOFIBROSIS", "Idiopathic myelofibrosis", "CIMF", "myelosclerosis with myeloid metaplasia", "AMM", "acute myeloid leukemia", "AML - acute Myeloid Leukemia", "Leukemia, Myelocytic, acute", "acute myeloblastic leukemia", "acute myelogenous leukemia", "Acute myelogenous leukemia; AML", "Acute Granulocytic Leukemia", "LEUKEMIA, ACUTE MYELOID; AML", "Acute non lymphoblastic leukemia", "myeloid leukemia, acute", "LEUKEMIA, ACUTE MYELOID", "ANLL", "Hematopoeitic - Acute Myleogenous Leukemia (AML)", "Acute Myeloid Leukemia", "Leukemia, Acute Myeloid, Susceptibility to", "Acute Myeloid Leukemia (AML)", "Leukemia, Acute Myelogenous", "Acute Myelogenous Leukemias", "AML", "Acute Nonlymphocytic Leukemia", "Acute Myelocytic Leukemia", "acute myeloid leukaemia"]}
-{"question": "Gene BIK has a genetic association with diseases such as", "references": ["prostate cancer", "malignant tumor of the prostate", "prostatic cancer", "tumor of the prostate", "malignant neoplasm of the prostate", "prostate cancer, familial", "hereditary prostate cancer"]}
-{"question": "Gene TREM2 has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene ATP2B2 has a genetic association with diseases such as", "references": ["amyotrophic lateral sclerosis", "ALS", "Lou Gehrig's disease", "motor neuron disease, bulbar", "Lou Gehrig disease", "Charcot disease", "Amyotrophic lateral sclerosis", "motor neurone disease", "Lou Gehrig's disease"]}
-{"question": "Gene GCDH has a genetic association with diseases such as", "references": ["glutaric aciduria type 1", "glutaryl-CoA dehydrogenase deficiency", "GA1", "glutaric acidemia type 1", "GCDHD", "GLUTARIC ACIDEMIA I", "Glutaryl-coenzyme A dehydrogenase deficiency", "Glutaric Aciduria 1", "Ga 1", "Glutaric Aciduria, Type 1", "Glutaric aciduria type 1", "glutaric acidemia I", "glutaric aciduria type I", "glutaric aciduria 1", "glutaryl-coenzyme A dehydrogenase deficiency", "glutaric academia type 1", "glutaryl-coA dehydrogenase deficiency"]}
-{"question": "Gene SPATA13 has a genetic association with diseases such as", "references": ["cleft lip and cleft palate", "cleft palate", "cleft lip", "cheilopalatoschisis", "Complete unilateral cleft palate with cleft lip (disorder)", "Unilateral complete cleft palate with cleft lip", "Unilateral complete cleft palate with cleft lip (disorder)", "Unilateral incomplete cleft palate with cleft lip", "Unilateral incomplete cleft palate with cleft lip (disorder)", "cleft palate with cleft lip, unilateral, complete", "cleft palate with cleft lip, unilateral, incomplete", "incomplete unilateral cleft palate with cleft lip (disorder)", "orofacial cleft", "obsolete cheilopalatoschisis", "alcohol dependence", "alcoholism", "alcohol dependence syndrome", "alcohol addiction"]}
-{"question": "Gene KSR2 has a genetic association with diseases such as", "references": ["endometriosis"]}
-{"question": "Gene Coffin-Siris syndrome has a genetic association with diseases such as", "references": ["ARID1B", "6A3-5", "BAF250B", "BRIGHT", "DAN15", "ELD/OSA1", "MRD12", "OSA2", "P250R", "CSS1", "AT-rich interaction domain 1B", "SMARCF2"]}
-{"question": "Gene Bulbar palsy has a genetic association with diseases such as", "references": ["SLC52A3", "BVVLS", "BVVLS1", "C20orf54", "RFT2", "RFVT3", "bA371L19.1", "hRFT2", "solute carrier family 52 member 3"]}
-{"question": "Gene FOXP4 has a genetic association with diseases such as", "references": ["prostate cancer", "malignant tumor of the prostate", "prostatic cancer", "tumor of the prostate", "malignant neoplasm of the prostate", "prostate cancer, familial", "hereditary prostate cancer"]}
-{"question": "Gene TJP2 has a genetic association with diseases such as", "references": ["refractive error", "disorder of refraction", "eye refraction disorder", "refractive disorder", "ametropia", "refraction or accommodation disorder", "refraction error", "Abnormality of refraction", "Refractive errors"]}
-{"question": "Gene ADA2 has a genetic association with diseases such as", "references": ["Sneddon syndrome", "Idiopathic livedo reticularis with systemic involvement (disorder)", "Idiopathic livedo reticularis with systemic involvement", "Livedo racemosa-cerebrovascular accident syndrome", "Livedo reticularis-cerebrovascular accident syndrome", "Livedo Reticularis and Cerebrovascular Accidents", "Ehrmann-Sneddon syndrome", "Sneddon's syndrome", "SNEDDON SYNDROME", "Livedo racemosa and cerebrovascular accidents", "Cerebro-vascular lesions and livedo reticularis"]}
-{"question": "Gene CEBPE has a genetic association with diseases such as", "references": ["acute lymphocytic leukemia", "ALL", "acute lymphoblastic leukemia", "acute lymphoblastic leukaemia"]}
-{"question": "Gene PMS2 has a genetic association with diseases such as", "references": ["Lynch syndrome", "COCA 1", "HNPCC - hereditary nonpolyposis colon cancer", "Hereditary Defective Mismatch Repair syndrome", "hereditary non-polyposis colon cancer type 1", "hereditary nonpolyposis colorectal cancer", "hereditary nonpolyposis colorectal neoplasm", "hereditary nonpolyposis colon cancer", "HNPCC", "Hereditary Nonpolyposis Colorectal Cancer", "Familial nonpolyposis colon cancer", "Familial nonpolyposis colorectal cancer", "colorectal neoplasm, hereditary nonpolyposis", "Colorectal Neoplasms, Hereditary Nonpolyposis", "Mismatch repair cancer syndrome", "Turcot syndrome", "Childhood Cancer Syndrome", "MMRCS", "CMMR-D", "Btp1 Syndrome", "CMMR-D syndrome", "Mismatch Repair Deficiency", "MISMATCH REPAIR CANCER SYNDROME; MMRCS", "Mmr Deficiency", "Brain Tumor-Polyposis Syndrome 1", "MISMATCH REPAIR CANCER SYNDROME", "Constitutional Mis-Match Repair Deficiency Syndrome", "Constitutional Mismatch Repair Deficiency Syndrome"]}
-{"question": "Gene SLC6A5 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene multiple myeloma has a genetic association with diseases such as", "references": ["TNFRSF13B", "CD267", "CVID", "CVID2", "RYZN", "TACI", "TNFRSF14B", "IGAD2", "tumor necrosis factor receptor superfamily member 13B", "TNF receptor superfamily member 13B", "CBX7", "chromobox 7", "CCND1", "BCL1", "D11S287E", "PRAD1", "U21B31", "cyclin D1", "DNAH11", "CILD7", "DNAHBL", "DNAHC11", "DNHBL", "DPL11", "dynein axonemal heavy chain 11", "DTNB", "dystrobrevin beta"]}
-{"question": "Gene HMBOX1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene CHARGE syndrome has a genetic association with diseases such as", "references": ["CHD7", "CRG", "HH5", "IS3", "KAL5", "chromodomain helicase DNA binding protein 7"]}
-{"question": "Gene APBB2 has a genetic association with diseases such as", "references": ["dental caries", "dental caries extending into pulp", "dental caries of smooth surface", "dental caries pit and fissure", "tooth decay", "cavities", "caries"]}
-{"question": "Gene PIK3R1 has a genetic association with diseases such as", "references": ["SHORT syndrome", "Short Stature, Hyperextensibility, Hernia, Ocular Depression, Rieger Anomaly, and Teething Delay", "SHORT SYNDROME", "Rieger anomaly-partial lipodystrophy syndrome", "Aarskog-Ose-Pande syndrome", "Lipodystrophy, Partial, With Rieger Anomaly and Short Stature", "Lipodystrophy-Rieger anomaly-diabetes syndrome", "PASLI Disease", "IMD36", "immunodeficiency 36", "immunodeficiency type 36", "senescent T-cells-lymphadenopathy-immunodeficiency syndrome due to p110delta-activating mutation", "PIK3R1-associated immunodeficiency"]}
-{"question": "Gene ADCY8 has a genetic association with diseases such as", "references": ["post-traumatic stress disorder", "PTSD", "traumatic neurosis", "posttraumatic stress disorder", "Stress Disorders, Post-Traumatic", "post traumatic stress disorder"]}
-{"question": "Gene ZNF577 has a genetic association with diseases such as", "references": ["breast cancer", "malignant neoplasm of breast", "malignant tumor of the breast", "mammary cancer", "primary breast cancer", "breast disorder"]}
-{"question": "Gene Crigler-Najjar syndrome has a genetic association with diseases such as", "references": ["UGT1A1", "BILIQTL1", "GNT1", "HUG-BR1", "UDPGT", "UDPGT 1-1", "UGT1", "UGT1A", "UDP glucuronosyltransferase family 1 member A1"]}
-{"question": "Gene alveolar rhabdomyosarcoma has a genetic association with diseases such as", "references": ["PAX7", "HUP1", "PAX7B", "RMS2", "Pax7", "paired box 7", "MYOSCO", "FOXO1", "FKH1", "FKHR", "FOXO1A", "forkhead box O1", "PAX3", "CDHS", "HUP2", "WS1", "WS3", "Pax3", "paired box 3"]}
-{"question": "Gene glucocorticoid-remediable aldosteronism has a genetic association with diseases such as", "references": ["CYP11B2", "ALDOS", "CPN2", "CYP11B", "CYP11BL", "CYPXIB2", "P-450C18", "P450C18", "P450aldo", "cytochrome P450 family 11 subfamily B member 2"]}
-{"question": "Gene PCLO has a genetic association with diseases such as", "references": ["major depressive disorder", "recurrent depressive disorder", "major depression", "unipolar depression", "MDD", "clinical depression", "recurrent major depression", "single major depressive episode", "recurrent major depression in complete remission", "recurrent major depressive episodes, in full remission (disorder)", "major depression disorder", "depression"]}
-{"question": "Gene ventricular septal defect has a genetic association with diseases such as", "references": ["GATA4", "GATA binding protein 4", "ASD2", "TACHD", "VSD1", "TOF", "CITED2", "ASD8", "MRG-1", "MRG1", "P35SRJ", "VSD2", "Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 2"]}
-{"question": "Gene Klippel-Feil syndrome has a genetic association with diseases such as", "references": ["MEOX1", "KFS2", "MOX1", "mesenchyme homeobox 1", "GDF6", "BMP-13", "BMP13", "CDMP2", "KFM", "KFS", "KFS1", "KFSL", "LCA17", "MCOP4", "MCOPCB6", "SCDO4", "SGM1", "growth differentiation factor 6", "SYNS4", "GDF3", "KFS3", "MCOP7", "MCOPCB6", "growth differentiation factor 3"]}
-{"question": "Gene Ritscher\u2013Schinzel syndrome has a genetic association with diseases such as", "references": ["WASHC5", "RTSC", "SPG8", "RTSC1", "KIAA0196", "WASH complex subunit 5"]}
-{"question": "Gene Fuchs' endothelial dystrophy has a genetic association with diseases such as", "references": ["TCF4", "E2-2", "ITF-2", "ITF2", "PTHS", "SEF-2", "SEF2", "SEF2-1", "SEF2-1A", "SEF2-1B", "SEF2-1D", "TCF-4", "bHLHb19", "FECD3", "transcription factor 4", "CDG2T", "PTPRG", "HPTPG", "PTPG", "R-PTP-GAMMA", "RPTPG", "protein tyrosine phosphatase, receptor type G", "protein tyrosine phosphatase receptor type G"]}
-{"question": "Gene STARD13 has a genetic association with diseases such as", "references": ["intracranial aneurysm", "brain aneurysm", "Intracranial aneurysm", "cerebral aneurysm"]}
-{"question": "Gene CDYL2 has a genetic association with diseases such as", "references": ["breast cancer", "malignant neoplasm of breast", "malignant tumor of the breast", "mammary cancer", "primary breast cancer", "breast disorder"]}
-{"question": "Gene Immunodeficiency 26 has a genetic association with diseases such as", "references": ["PRKDC", "DNA-PKcs", "DNAPK", "DNPK1", "HYRC", "HYRC1", "XRCC7", "p350", "IMD26", "protein kinase, DNA-activated, catalytic polypeptide", "DNA-PKC", "protein kinase, DNA-activated, catalytic subunit", "DNAPKc"]}
-{"question": "Gene Majewski's polydactyly syndrome has a genetic association with diseases such as", "references": ["NEK1", "NY-REN-55", "SRPS2", "SRPS2A", "SRTD6", "NIMA related kinase 1", "ALS24"]}
-{"question": "Gene PITX1 has a genetic association with diseases such as", "references": ["clubfoot", "Congenital equinovarus", "Equinovarus deformity of foot (finding)", "congenital clubfoot", "congenital talipes equinovarus", "Club foot, talipes equinovarus", "Equinovarus deformity of foot", "CLUBFOOT, CONGENITAL, WITH OR WITHOUT DEFICIENCY OF LONG BONES AND/OR MIRROR-IMAGE POLYDACTYLY", "Club Foot", "CLUBFOOT, CONGENITAL, WITH OR WITHOUT DEFICIENCY OF LONG BONES AND/OR MIRROR-IMAGE POLYDACTYLY; CCF", "Talipes Equinovarus", "Talipes", "CCF", "Clubbed Foot", "Liebenberg syndrome", "carpal synostosis with dysplastic elbow joints and brachydactyly", "LIEBENBERG SYNDROME; LBNBG", "LIEBENBERG SYNDROME", "LBNBG", "Synostosis, Carpal, With Dysplastic Elbow Joints and Brachydactyly", "Brachydactyly elbow wrist dysplasia", "Brachydactyly-joint dysplasia syndrome", "brachydactyly with joint dysplasia"]}
-{"question": "Gene arrhythmogenic right ventricular cardiomyopathy has a genetic association with diseases such as", "references": ["TGFB3", "ARVD", "ARVD1", "RNHF", "TGF-beta3", "Transforming growth factor, beta 3", "LDS5", "transforming growth factor beta 3", "TGF beta 3", "DSG2", "ARVC10", "ARVD10", "CDHF5", "CMD1BB", "HDGC", "desmoglein 2", "PKP2", "ARVD9", "plakophilin 2"]}
-{"question": "Gene endometrial cancer has a genetic association with diseases such as", "references": ["ADAM12", "ADAM12-OT1", "CAR10", "MCMP", "MCMPMltna", "MLTN", "MLTNA", "ADAM metallopeptidase domain 12", "LINGO2", "LERN3", "LRRN6C", "leucine rich repeat and Ig domain containing 2", "CACNA2D3", "HSA272268", "calcium voltage-gated channel auxiliary subunit alpha2delta 3"]}
-{"question": "Gene JAKMIP3 has a genetic association with diseases such as", "references": ["chronic obstructive pulmonary disease", "COPD", "chronic obstructive airway disease", "chronic obstructive airways disease NOS", "chronic obstructive lung disease", "chronic obstructive airways disease NOS disorder", "chronic obstructive lung disease disorder", "COLD", "COLD (chronic obstructive lung disease)", "Chronic Obstructive Pulmonary Disease, (COPD)", "Pulmonary Disease (COPD), Chronic Obstructive", "Obstructive Pulmonary Disease (COPD), Chronic", "Chronic Obstructive Airways Disease", "Disease (COPD), Chronic Obstructive", "Chronic Obstructive Pulmonary Disease (COPD)", "obstructive lung disease, chronic", "COPD, Chronic Obstructive Pulmonary Disease", "Pulmonary Disease, Chronic Obstructive"]}
-{"question": "Gene KRT83 has a genetic association with diseases such as", "references": ["monilethrix", "Moniliform hair syndrome", "Nodose hair", "MNLIX", "MONILETHRIX", "MONILETHRIX; MNLIX", "Beaded hair"]}
-{"question": "Gene HERPUD1 has a genetic association with diseases such as", "references": ["metabolic disease", "metabolic illness", "disorder of metabolic process", "metabolic disorder", "metabolic diseases", "disease of metabolism"]}
-{"question": "Gene GRID2 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene Estrogen insensitivity syndrome has a genetic association with diseases such as", "references": ["ESR1", "ER", "ESR", "ESRA", "ESTRR", "Era", "NR3A1", "estrogen receptor 1"]}
-{"question": "Gene IL13 has a genetic association with diseases such as", "references": ["asthma", "exercise-induced asthma", "chronic obstructive asthma", "chronic obstructive asthma with status asthmaticus", "chronic obstructive asthma with acute exacerbation", "bronchial hyperreactivity", "Exercise induced asthma", "Asthma", "asthma brionchiole", "Hodgkin lymphoma", "HL", "Hodgkin disease", "Hodgkin's sarcoma", "Hodgkins lymphoma", "stage I Subdiaphragmatic Hodgkin Lymphoma", "stage II Subdiaphragmatic Hodgkin Lymphoma", "Hodgkin's lymphoma; HL", "Hodgkin's disease", "Hodgkin's lymphoma", "psoriasis"]}
-{"question": "Gene Niemann\u2013Pick disease, type C has a genetic association with diseases such as", "references": ["NPC1", "NPC", "NPC intracellular cholesterol transporter 1", "SLC65A1", "POGZ"]}
-{"question": "Gene ABCD syndrome has a genetic association with diseases such as", "references": ["EDNRB", "ABCDS", "ET-B", "ET-BR", "ETB", "ETBR", "ETRB", "HSCR", "HSCR2", "WS4A", "ETB1", "endothelin receptor type B"]}
-{"question": "Gene MECP2 has a genetic association with diseases such as", "references": ["Angelman syndrome", "happy puppet syndrome", "puppetlike syndrome", "AS", "Happy Puppet Syndrome, Formerly", "Angelman Syndrome Chromosome Region", "Rett syndrome", "Rett's disorder", "cerebroatrophic hyperammonemia", "atypical Rett syndrome", "Rett's syndrome"]}
-{"question": "Gene CDH4 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene Tumoral calcinosis has a genetic association with diseases such as", "references": ["FGF23", "ADHR", "FGFN", "HPDR2", "HYPF", "PHPTC", "fibroblast growth factor 23", "HFTC2", "GALNT3", "GalNAc-T3", "HFTC", "HHS", "polypeptide N-acetylgalactosaminyltransferase 3", "HFTC1"]}
-{"question": "Gene persistent M\u00fcllerian duct syndrome has a genetic association with diseases such as", "references": ["AMHR2", "AMHR", "MISR2", "MISRII", "MRII", "anti-Mullerian hormone receptor type 2"]}
-{"question": "Gene LGR4 has a genetic association with diseases such as", "references": ["osteoporosis", "bone loss"]}
-{"question": "Gene ovarian cancer has a genetic association with diseases such as", "references": ["SKAP1", "HEL-S-81p", "SCAP1", "SKAP55", "src kinase associated phosphoprotein 1", "MUTYH", "MYH", "mutY DNA glycosylase", "mutY homolog (E. coli)", "RAD51C", "BROVCA3", "FANCO", "R51H3", "RAD51L2", "RAD51 paralog C", "RAD51D", "BROVCA4", "R51H3", "RAD51L3", "TRAD", "RAD51 paralog D"]}
-{"question": "Gene CHRNG has a genetic association with diseases such as", "references": ["multiple pterygium syndrome", "Multiple pterygium syndrome Escobar type", "Pterygium universale", "Autosomal recessive multiple pterygium syndrome", "MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT", "Multiple pterygium syndrome", "Autosomal recessive non-lethal multiple pterygium syndrome", "EVMPS", "Multiple Pterygium Syndrome, Nonlethal Type", "MULTIPLE PTERYGIUM SYNDROME, ESCOBAR VARIANT; EVMPS", "Multiple pterygium syndrome nonlethal type", "Pterygium colli syndrome", "multiple pterygium syndrome, autosomal recessive", "Pterygium Syndrome", "Escobar variant multiple pterygium syndrome", "Escobar syndrome"]}
-{"question": "Gene Bart-Pumphrey syndrome has a genetic association with diseases such as", "references": ["GJB2", "CX26", "DFNA3", "DFNA3A", "DFNB1", "DFNB1A", "HID", "KID", "NSRD1", "PPK", "gap junction protein beta 2", "BAPS"]}
-{"question": "Gene ATP6V0A2 has a genetic association with diseases such as", "references": ["Wrinkly skin syndrome", "WSS", "Wrinkled skin syndrome", "WRINKLY SKIN SYNDROME", "WRINKLY SKIN SYNDROME; WSS"]}
-{"question": "Gene Guillain\u2013Barr\u00e9 Syndrome has a genetic association with diseases such as", "references": ["PMP22", "CMT1A", "CMT1E", "DSS", "GAS-3", "HMSNIA", "HNPP", "Sujojp110", "GAS3", "peripheral myelin protein 22", "CIDP", "Sp110"]}
-{"question": "Gene FHL5 has a genetic association with diseases such as", "references": ["migraine", "migraine variant", "sick headache", "migraine with or without aura", "migraine disorders", "migraine disorder"]}
-{"question": "Gene multiple pterygium syndrome has a genetic association with diseases such as", "references": ["CHRNG", "ACHRG", "cholinergic receptor nicotinic gamma subunit", "MYH3", "HEMHC", "MYHC-EMB", "MYHSE1", "SMHCE", "DA2A", "DA2B", "DA8", "myosin, heavy chain 3, skeletal muscle, embryonic", "myosin heavy chain 3", "CPSKF1A", "DA2B3", "CPSKF1B", "CPSFS1B", "CPSFS1A", "CHRND", "ACHRD", "CMS2A", "FCCMS", "SCCMS", "CMS3A", "CMS3B", "CMS3C", "cholinergic receptor nicotinic delta subunit", "CHRNA1", "ACHRA", "ACHRD", "CHRNA", "CMS2A", "FCCMS", "SCCMS", "CMS1A", "CMS1B", "Cholinergic receptor, nicotinic, alpha 1", "cholinergic receptor nicotinic alpha 1 subunit"]}
-{"question": "Gene optic atrophy-intellectual disability syndrome has a genetic association with diseases such as", "references": ["NR2F1", "BBOAS", "BBSOAS", "COUP-TFI", "EAR-3", "EAR3", "ERBAL3", "NR2F2", "SVP44", "TCFCOUP1", "TFCOUP1", "nuclear receptor subfamily 2 group F member 1", "COUPTF1"]}
-{"question": "Gene FSHR has a genetic association with diseases such as", "references": ["polycystic ovary syndrome", "Multicystic ovaries", "PCOS", "Polycystic Ovarian disease", "Polycystic ovaries", "Polycystic ovary syndrome", "Stein-Leventhal synd.", "Stein-Leventhal syndrome", "polycystic ovary", "polysistic ovary syndrom", "Hyperandrogenemia", "PCOS1", "POLYCYSTIC OVARY SYNDROME 1; PCOS1", "Pco1", "POLYCYSTIC OVARY SYNDROME 1", "prostate cancer", "malignant tumor of the prostate", "prostatic cancer", "tumor of the prostate", "malignant neoplasm of the prostate", "prostate cancer, familial", "hereditary prostate cancer", "erectile dysfunction", "Sexual impotence (finding)", "Erectile Dysfunction", "ED", "Erectile Dysfunction; ED", "Sexual impotence", "Male Impotence", "Male Sexual Impotence", "Dysfunction, Erectile", "impotence", "Impotence, Male Sexual", "Sexual Impotence, Male", "Impotence, Male", "46 XX gonadal dysgenesis", "OVARIAN DYSGENESIS 1; ODG1", "XX GONADAL DYSGENESIS", "XXGD", "Ovarian Dysgenesis, Hypergonadotropic, Autosomal Recessive", "OVARIAN FAILURE, HYPERGONADOTROPIC", "ODG1", "GONADAL DYSGENESIS, XX TYPE", "Gonadal Dysgenesis, 20 Type", "Ovarian Dysgenesis, Hypergonadotropic, With Normal Karyotype", "ovarian dysgenesis", "ovarian hyperstimulation syndrome", "secondary Meig's syndrome", "OHSS", "Ovarian Hyperstimulation Syndrome, Familial Gestational Spontaneous"]}
-{"question": "Gene DLG2 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "nephroblastoma", "Wilms tumor", "adult nephroblastoma", "adult renal Wilms' tumor", "childhood renal Wilms' cancer", "renal Wilms tumor", "Wilms' tumor", "childhood renal Wilms tumor", "Wilms\u2019 tumour", "Wilm's tumour", "Wilm's tumor", "Wilms tumour", "Parkinson's disease", "paralysis agitans", "parkinsonismus idiopathicus", "Parkinson", "Parkinson disease"]}
-{"question": "Gene hypoplastic left heart syndrome has a genetic association with diseases such as", "references": ["NKX2-5", "CHNG5", "CSX", "CSX1", "HLHS2", "NKX2.5", "NKX2E", "NKX4-1", "VSD3", "NK2 homeobox 5", "GJA1", "AVSD3", "CMDR", "CX43", "EKVP", "GJAL", "HLHS1", "HSS", "ODDD", "PPKCA", "gap junction protein alpha 1", "EKVP3"]}
-{"question": "Gene FADS1 has a genetic association with diseases such as", "references": ["metabolic disease", "metabolic illness", "disorder of metabolic process", "metabolic disorder", "metabolic diseases", "disease of metabolism"]}
-{"question": "Gene BMP2 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene OASL has a genetic association with diseases such as", "references": ["cardiovascular disease", "CV disease", "cardiovascular system disease", "myocardiovascular system disease", "heart, respiratory, and blood vessel disease", "diseases of the circulatory system", "cardiovascular diseases", "disease of subdivision of hemolymphoid system", "CVD"]}
-{"question": "Gene CAMK4 has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene CLEC16A has a genetic association with diseases such as", "references": ["systemic lupus erythematosus", "SLE", "lupus", "Lupus Erythematosus, systemic", "SLE - Lupus Erythematosus, systemic", "disseminated lupus erythematosus", "Systemic lupus erythematosus", "obesity", "corpulence", "overfatness", "fatness", "obese", "atopic dermatitis", "Allergic (intrinsic) eczema (disorder)", "Atopic dermatitis", "Atopic dermatitis (disorder)", "Atopic dermatitis NOS (disorder)", "Atopic neurodermatitis (disorder)", "Besnier's prurigo", "Besnier's prurigo (disorder)", "allergic dermatitis", "atopic eczema", "atopic dermatitis and related conditions", "Atopic neurodermatitis", "Allergic", "allergic rhinitis", "allergic rhinitis due to animal (cat) (dog) hair and dander", "allergic rhinitis due to food", "atopic rhinitis", "pollenosis", "Allergic rhinitis due to pollen", "Allergic rhinitis due to pollen (disorder)", "Allergy to pollen (disorder)", "Hay fever - pollens", "Non-seasonal allergic rhinitis", "Perenial allergic rhinitis", "Pollinosis", "hfcy", "Rhinitis, Allergic", "multiple sclerosis", "MS", "encephalomyelitis disseminata", "insular sclerosis", "disseminated sclerosis", "generalized multiple sclerosis", "Generalized multiple sclerosis (disorder)", "generalised multiple sclerosis", "Multiple sclerosis; MS", "Multiple sclerosis", "type-1 diabetes", "IDDM", "insulin-dependent diabetes mellitus", "type I diabetes mellitus", "T1DM", "insulin dependent diabetes", "juvenile diabetes", "diabetes mellitus juvenile type", "DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM", "Diabetes Mellitus, Type 1", "Diabetes Mellitus, Insulin-Dependent, 1", "DIABETES MELLITUS, INSULIN-DEPENDENT", "Juvenile-Onset Diabetes", "Insulin-Dependent Diabetes Mellitus 1", "diabetes (type 1)", "type 1 diabetes mellitus", "primary biliary cirrhosis", "biliary liver cirrhosis", "cholestatic cirrhosis", "chronic nonsuppurative destructive cholangitis", "primary biliary cholangitis", "PBC", "Primary biliary cirrhosis", "Primary biliary cholangitis", "Liver Cirrhosis, Biliary"]}
-{"question": "Gene FGF1 has a genetic association with diseases such as", "references": ["hypertrophic cardiomyopathy", "familial hypertrophic cardiomyopathy", "hypertrophic obstructive cardiomyopathy", "HCM", "hypertrophic heart disease", "Hypertrophic cardiomyopathy", "Cardiomyopathy, Hypertrophic"]}
-{"question": "Gene PEX26 has a genetic association with diseases such as", "references": ["Zellweger spectrum disorder", "Peroxisomal Biogenesis Disorders", "Zellweger Syndrome Spectrum", "Cerebrohepatorenal Syndrome", "ZSS", "Peroxisome biogenesis disorders-Zellweger spectrum disorders", "peroxisome biogenesis disorder", "peroxisome biogenesis disorders, Zellweger syndrome spectrum", "PBD-ZSD", "Zellweger syndrome spectrum", "Peroxisome biogenesis disorder spectrum", "ZSD", "Zellweger spectrum", "PBD, ZSS", "cerebrohepatorenal syndrome", "Zellweger spectrum disorder", "Peroxisome biogenesis disorder", "obsolete Zellweger spectrum disorder"]}
-{"question": "Gene CAMK2B has a genetic association with diseases such as", "references": ["osteoarthritis", "degenerative arthritis", "degenerative joint disease", "hypertrophic arthritis", "osteoarthrosis", "osteoarthrosis and allied disorder", "metabolic disease", "metabolic illness", "disorder of metabolic process", "metabolic disorder", "metabolic diseases", "disease of metabolism"]}
-{"question": "Gene GABRG3 has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene Succinyl-CoA:3-oxoacid CoA transferase deficiency has a genetic association with diseases such as", "references": ["OXCT1", "OXCT", "SCOT", "3-oxoacid CoA-transferase 1"]}
-{"question": "Gene DSG2 has a genetic association with diseases such as", "references": ["arrhythmogenic right ventricular cardiomyopathy", "arrhythmogenic right ventricular dysplasia/cardiomyopathy", "ARVC", "ARVC cardiomyopathy", "ARVD", "arrhythmogenic right ventricular dysplasia", "Arrhythmogenic RVD", "Right Ventricular Dysplasia"]}
-{"question": "Gene CYP27A1 has a genetic association with diseases such as", "references": ["cerebrotendinous xanthomatosis", "Van Bogaert\u2013Scherer\u2013Epstein syndrome", "Cholestanol storage disease (disorder)", "Cholestanol storage disease", "CEREBROTENDINOUS XANTHOMATOSIS", "CEREBROTENDINOUS XANTHOMATOSIS; CTX", "CTX", "Sterol 27-hydroxylase deficiency", "Cerebral Cholesterinosis", "Xanthomatosis, Cerebrotendinous"]}
-{"question": "Gene adenocarcinoma of the lung has a genetic association with diseases such as", "references": ["TERT", "CMM9", "DKCA2", "DKCB4", "EST2", "PFBMFT1", "TCS1", "TP2", "TRT", "hEST2", "hTRT", "telomerase reverse transcriptase", "HTERT", "TP63", "AIS", "B(p51A)", "B(p51B)", "EEC3", "KET", "LMS", "NBP", "OFC8", "RHS", "SHFM4", "TP53CP", "TP53L", "TP73L", "p40", "p51", "p53CP", "p63", "p73H", "p73L", "tumor protein p63", "BPTF", "FAC1", "FALZ", "NURF301", "bromodomain PHD finger transcription factor", "NEDDFL", "BTNL2", "BTL-II", "BTN7", "HSBLMHC1", "SS2", "butyrophilin like 2", "CLPTM1L", "CRR9", "CLPTM1-like", "CLPTM1 like"]}
-{"question": "Gene allergic rhinitis has a genetic association with diseases such as", "references": ["ENTPD6", "CD39L2", "IL-6SAG", "IL6ST2", "NTPDase-6", "dJ738P15.3", "ectonucleoside triphosphate diphosphohydrolase 6 (putative)", "ectonucleoside triphosphate diphosphohydrolase 6", "CLEC16A", "Gop-1", "KIAA0350", "C-type lectin domain family 16 member A", "C-type lectin domain containing 16A", "GLI3", "ACLS", "GCPS", "GLI3-190", "GLI3FL", "PAP-A", "PAPA", "PAPA1", "PAPB", "PHS", "PPDIV", "GLI family zinc finger 3", "TSLP", "thymic stromal lymphopoietin"]}
-{"question": "Gene colorectal cancer has a genetic association with diseases such as", "references": ["TCF7L2", "TCF-4", "TCF4", "transcription factor 7 like 2", "SMAD7", "CRCS3", "MADH7", "MADH8", "SMAD family member 7", "RHPN2", "P76RBE", "RHOBP", "rhophilin, Rho GTPase binding protein 2", "rhophilin Rho GTPase binding protein 2", "PNMA8A", "PNMAL1", "FLJ10781", "paraneoplastic Ma antigen family member 8A", "PNMA family member 8A", "MORC1", "CT33", "MORC", "ZCW6", "MORC family CW-type zinc finger 1", "DPP6", "DPPX", "VF2", "MRD33", "DPL1", "dipeptidyl peptidase like 6", "LAMC1", "LAMB2", "Laminin, gamma 1", "laminin subunit gamma 1", "CCND2", "KIAK0002", "MPPH3", "cyclin D2", "TBX3", "TBX3-ISO", "UMS", "XHL", "T-box 3", "T-box transcription factor 3", "CCDC190", "C1orf110", "coiled-coil domain containing 190", "POLD3", "P66", "P68", "PPP1R128", "polymerase (DNA) delta 3, accessory subunit", "DNA polymerase delta 3, accessory subunit", "SLC22A3", "EMT", "EMTH", "OCT3", "solute carrier family 22 member 3", "LAMA5", "Laminin, alpha 5", "laminin subunit alpha 5", "CDH1", "Arc-1", "CD324", "CDHE", "ECAD", "LCAM", "UVO", "cadherin 1", "BCDS1", "GNAS", "AHO", "C20orf45", "GNAS1", "GPSA", "GSA", "GSP", "NESP", "POH", "SCG6", "SgVI", "GNAS complex locus", "PITA3", "AKT1", "AKT", "CWS6", "PKB", "PKB-ALPHA", "PRKBA", "RAC", "RAC-ALPHA", "AKT serine/threonine kinase 1", "MSH6", "mutS homolog 6", "GTBP", "GTMBP", "HNPCC5", "HSAP", "p160", "MMRCS3", "PIK3CA", "CLOVE", "CWS5", "MCAP", "MCM", "MCMTC", "PI3K", "p110-alpha", "PI3K-alpha", "phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha", "CLAPO", "CCM4", "WRN", "RECQ3", "RECQL2", "RECQL3", "Werner syndrome RecQ like helicase", "WRN RecQ like helicase", "SMAD3", "HSPC193", "HsT17436", "JV15-2", "LDS1C", "LDS3", "MADH3", "SMAD family member 3", "MLH3", "HNPCC7", "mutL homolog 3", "AXIN2", "AXIL", "ODCRCS", "axin 2", "MSH2", "mutS homolog 2", "COCA1", "FCC1", "HNPCC", "HNPCC1", "LCFS2", "hMSH2", "MMRCS2", "BRAF", "B-RAF1", "BRAF1", "NS7", "RAFB1", "B-Raf", "B-Raf proto-oncogene, serine/threonine kinase", "ALOX12", "12-LOX", "12S-LOX", "LOG12", "arachidonate 12-lipoxygenase, 12S type", "MLH1", "mutL homolog 1", "COCA2", "FCC2", "HNPCC", "HNPCC2", "hMLH1", "EPHA3", "Epha3", "AW492086", "Cek4", "ETK1", "End3", "Hek", "Hek4", "Mek4", "Tyro4", "EK4", "ETK", "EPH receptor A3", "HEK", "HEK4", "TYRO4", "COX1", "mitochondrially encoded cytochrome c oxidase I", "COI", "MTCO1", "Main subunit of cytochrome c oxidase", "CO I", "cytochrome c oxidase subunit I"]}
-{"question": "Gene FARP1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "fatty liver disease", "hepatic lipidosis", "fatty degeneration of the liver", "steatosis of the liver", "Fatty liver disease", "fatty change of liver", "steatosis of liver (disorder)", "steatosis of liver", "liver steatosis", "hepatic steatosis", "fatty liver"]}
-{"question": "Gene congenital heart disease has a genetic association with diseases such as", "references": ["TAB2", "CHTD2", "MAP3K7IP2", "TAB-2", "TGF-beta activated kinase 1/MAP3K7 binding protein 2", "TGF-beta activated kinase 1 (MAP3K7) binding protein 2"]}
-{"question": "Gene focal dermal hypoplasia has a genetic association with diseases such as", "references": ["PORCN", "DHOF", "FODH", "MG61", "PORC", "PPN", "porcupine homolog (Drosophila)", "porcupine O-acyltransferase"]}
-{"question": "Gene primary cutaneous amyloidosis has a genetic association with diseases such as", "references": ["IL31RA", "CRL", "CRL3", "GLM-R", "GLMR", "GPL", "IL-31RA", "PLCA2", "PRO21384", "hGLM-R", "interleukin 31 receptor A", "zcytoR17", "OSMR", "OSMRB", "PLCA1", "IL-31R-beta", "IL-31RB", "oncostatin M receptor", "OSMRbeta"]}
-{"question": "Gene RAD51B has a genetic association with diseases such as", "references": ["rheumatoid arthritis", "Arthritis or polyarthritis, rheumatic", "atrophic Arthritis", "Rheumatoid arthritis with vasculitis", "Malignant rheumatoid arthritis", "Rheumatoid arthritis", "male breast cancer", "malignant neoplasm of male breast", "neoplasm of male breast (disorder)"]}
-{"question": "Gene neuroacanthocytosis has a genetic association with diseases such as", "references": ["VPS13A", "CHAC", "CHOREIN", "vacuolar protein sorting 13 homolog A"]}
-{"question": "Gene Tourette syndrome has a genetic association with diseases such as", "references": ["PHEX", "HPDR", "HPDR1", "HYP", "HYP1", "LXHR", "PEX", "XLH", "phosphate regulating endopeptidase homolog, X-linked", "phosphate regulating endopeptidase homolog X-linked", "IMMP2L", "IMMP2L-IT1", "IMP2", "IMP2-LIKE", "inner mitochondrial membrane peptidase subunit 2", "SLITRK1", "LRRC12", "TTM", "SLIT and NTRK like family member 1", "slitrk1"]}
-{"question": "Gene RNF7 has a genetic association with diseases such as", "references": ["hepatitis C", "hep C", "NANBH", "Viral hepatitis C", "chronic hepatitis C", "hepatitis C infection", "hepatitis nonA nonB", "Non-A, Non-B Hepatitis", "hepatitis type C", "HCV"]}
-{"question": "Gene osteitis fibrosa cystica has a genetic association with diseases such as", "references": ["STX16", "SYN16", "syntaxin 16", "GNAS", "AHO", "C20orf45", "GNAS1", "GPSA", "GSA", "GSP", "NESP", "POH", "SCG6", "SgVI", "GNAS complex locus", "PITA3"]}
-{"question": "Gene PRKAR1A has a genetic association with diseases such as", "references": ["Carney complex", "Carney Complex, Type 1", "Carney Complex, Type 2", "Carney Syndrome", "LAMB Syndrome", "NAME Syndrome", "Carney complex variant", "CARNEY COMPLEX, TYPE 1; CNC1", "Myxoma, Spotty Pigmentation, and Endocrine Overactivity", "Carney Myxoma-Endocrine Complex", "CNC1"]}
-{"question": "Gene osteosarcoma has a genetic association with diseases such as", "references": ["ADAMTS6", "ADAM-TS 6", "ADAM-TS6", "ADAMTS-6", "ADAM metallopeptidase with thrombospondin type 1 motif 6"]}
-{"question": "Gene follicular thyroid cancer has a genetic association with diseases such as", "references": ["HRAS", "C-BAS/HAS", "C-H-RAS", "C-HA-RAS1", "CTLO", "H-RASIDX", "HAMSV", "HRAS1", "RASH1", "p21ras", "Harvey rat sarcoma viral oncogene homolog", "HRas proto-oncogene, GTPase", "Ki-Ras", "c-Ki-ras", "KRAS2", "KRAS", "c-K-ras", "RASK2", "NRAS", "ALPS4", "CMNS", "N-ras", "NCMS", "NRAS1", "NS6", "Neuroblastoma RAS viral oncogene homolog", "NRAS proto-oncogene, GTPase", "SRGAP1", "ARHGAP13", "NMTC2", "SLIT-ROBO Rho GTPase activating protein 1", "MINPP1", "HIPER1", "MINPP2", "MIPP", "multiple inositol-polyphosphate phosphatase 1", "PCH16"]}
-{"question": "Gene IMPA2 has a genetic association with diseases such as", "references": ["stroke", "CVA", "CVI", "brain attack", "embolic stroke", "cerebrovascular insult", "cerebrovascular disorder", "cerebrovascular accident", "cerebral vascular accident", "cerebrovascular disease", "cerebrovascular disorder", "Cerebrovascular accident (disorder)", "cerebrovascular accident", "CVA (cerebral vascular accident)", "CVA", "cerebrovascular disorders"]}
-{"question": "Gene FERMT3 has a genetic association with diseases such as", "references": ["attention deficit hyperactivity disorder", "ADHD", "hyperkinetic disorder", "attention deficit disorder", "AD/HD", "A.D.H.D", "attention deficit/hyperactivity disorder", "attention deficit hyperactivity syndrome", "Attention Deficit Disorder with Hyperactivity", "ADDH"]}
-{"question": "Gene FG syndrome has a genetic association with diseases such as", "references": ["MED12", "ARC240", "CAGH45", "FGS1", "HOPA", "MED12S", "OHDOX", "OKS", "OPA1", "TNRC11", "TRAP230", "mediator complex subunit 12", "Kto", "FLNA", "ABP-280", "ABPX", "CSBS", "CVD1", "FLN", "FLN-A", "FLN1", "FMD", "MNS", "NHBP", "OPD", "OPD1", "OPD2", "XLVD", "XMVD", "filamin A", "FGS2", "CASK", "CAGH39", "CAMGUK", "CMG", "FGS4", "LIN2", "MICPCH", "MRXSNA", "TNRC8", "calcium/calmodulin-dependent serine protein kinase (MAGUK family)", "calcium/calmodulin dependent serine protein kinase", "hCASK"]}
-{"question": "Gene MYO6 has a genetic association with diseases such as", "references": ["nonsyndromic deafness", "nonsyndromic hearing loss", "nonsyndromic hereditary hearing loss", "Familial deafness", "Non-syndromic genetic deafness", "Isolated genetic deafness"]}
-{"question": "Gene non-controlled substance abuse has a genetic association with diseases such as", "references": ["HIVEP1", "CIRIP", "CRYBP1", "GAAP", "MBP-1", "PRDII-BF1", "Schnurri-1", "ZAS1", "ZNF40", "ZNF40A", "human immunodeficiency virus type I enhancer binding protein 1", "HIVEP zinc finger 1", "PKNOX2", "PREP2", "PBX/knotted 1 homeobox 2", "KCND2", "KV4.2", "RK5", "potassium voltage-gated channel subfamily D member 2"]}
-{"question": "Gene Primrose syndrome has a genetic association with diseases such as", "references": ["ZBTB20", "DPZF", "HOF", "ODA-8S", "ZNF288", "PRIMS", "zinc finger and BTB domain containing 20"]}
-{"question": "Gene Kosaki overgrowth syndrome has a genetic association with diseases such as", "references": ["PDGFRB", "CD140B", "IBGC4", "IMF1", "JTK12", "PDGFR", "PDGFR-1", "PDGFR1", "KOGS", "PENTT", "platelet derived growth factor receptor beta"]}
-{"question": "Gene NBEAL1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene PORCN has a genetic association with diseases such as", "references": ["focal dermal hypoplasia", "Goltz syndrome", "Goltz-Gorlin Syndrome", "FOCAL DERMAL HYPOPLASIA; FDH", "Fodh", "FDH", "FOCAL DERMAL HYPOPLASIA"]}
-{"question": "Gene SPECC1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene SP110 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene DCLRE1C has a genetic association with diseases such as", "references": ["Omenn syndrome", "combined immunodeficiency with hypereosinophilia", "Severe Combined Immunodeficiency With Hypereosinophilia", "Reticuloendotheliosis, Familial, With Eosinophilia", "OMENN SYNDROME", "Reticuloendotheliosis familial with eosinophilia"]}
-{"question": "Gene ABCA7 has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease", "Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene NBN has a genetic association with diseases such as", "references": ["Nijmegen breakage syndrome", "Berlin breakage syndrome", "Microcephaly, normal intelligence and immunodeficiency (disorder)", "Seemanova syndrome", "Microcephaly, normal intelligence and immunodeficiency", "NBS", "AT V1", "Microcephaly-immunodeficiency-lymphoreticuloma syndrome", "Seemanova Syndrome 2", "Microcephaly With Normal Intelligence, Immunodeficiency, and Lymphoreticular Malignancies", "Ataxia-Telangiectasia Variant V2", "Nonsyndromal microcephaly autosomal recessive with normal intelligence", "Immunodeficiency, Microcephaly, and Chromosomal Instability", "Immunodeficiency-microcephaly-chromosomal instability syndrome", "Seemanova syndrome type 2", "Ataxia-telangiectasia, variant 1", "NIJMEGEN BREAKAGE SYNDROME", "Ataxia-Telangiectasia Variant V1", "Microcephaly with normal intelligence immunodeficiency and lymphoreticular malignancies", "Microcephaly immunodeficiency lymphoreticuloma", "Nonsyndromal Microcephaly, Autosomal Recessive, With Normal Intelligence", "ataxia telangiectasia variant 1 (AT-V1)"]}
-{"question": "Gene infantile myofibromatosis has a genetic association with diseases such as", "references": ["PDGFRB", "CD140B", "IBGC4", "IMF1", "JTK12", "PDGFR", "PDGFR-1", "PDGFR1", "KOGS", "PENTT", "platelet derived growth factor receptor beta", "NOTCH3", "CADASIL", "CASIL", "IMF2", "LMNS", "CADASIL1", "notch 3", "notch receptor 3"]}
-{"question": "Gene lung cancer has a genetic association with diseases such as", "references": ["CHEK2", "CDS1", "CHK2", "HuCds1", "LFS2", "PP1425", "RAD53", "hCds1", "checkpoint kinase 2", "TP63", "AIS", "B(p51A)", "B(p51B)", "EEC3", "KET", "LMS", "NBP", "OFC8", "RHS", "SHFM4", "TP53CP", "TP53L", "TP73L", "p40", "p51", "p53CP", "p63", "p73H", "p73L", "tumor protein p63", "BPTF", "FAC1", "FALZ", "NURF301", "bromodomain PHD finger transcription factor", "NEDDFL", "VTI1A", "MMDS3", "MVti1", "VTI1RP2", "Vti1-rp2", "vesicle transport through interaction with t-SNAREs 1A", "RAD52", "RAD52 homolog, DNA repair protein", "TERT", "CMM9", "DKCA2", "DKCB4", "EST2", "PFBMFT1", "TCS1", "TP2", "TRT", "hEST2", "hTRT", "telomerase reverse transcriptase", "HTERT", "MTMR3", "FYVE-DSP1", "ZFYVE10", "myotubularin related protein 3", "GPC5", "glypican 5", "CLPTM1L", "CRR9", "CLPTM1-like", "CLPTM1 like", "IL1RAP", "C3orf13", "IL-1RAcP", "IL1R3", "interleukin 1 receptor accessory protein"]}
-{"question": "Gene postural orthostatic tachycardia syndrome has a genetic association with diseases such as", "references": ["SLC6A2", "NAT1", "NET", "NET1", "SLC6A5", "solute carrier family 6 member 2", "Norepinephrine transporter", "norepinephrine transporter gene"]}
-{"question": "Gene ACTN2 has a genetic association with diseases such as", "references": ["periodontitis", "pyorrhea", "chronic pericementitis", "periodontium inflammation", "periodontiumitis"]}
-{"question": "Gene epidermolytic hyperkeratosis has a genetic association with diseases such as", "references": ["KRT1", "CK1", "EHK", "EHK1", "EPPK", "K1", "KRT1A", "NEPPK", "keratin 1", "KRT10", "BCIE", "BIE", "CK10", "EHK", "K10", "KPP", "keratin 10"]}
-{"question": "Gene CHL1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene Rotor syndrome has a genetic association with diseases such as", "references": ["SLCO1B1", "HBLRR", "LST-1", "LST1", "OATP-C", "OATP1B1", "OATP2", "OATPC", "SLC21A6", "solute carrier organic anion transporter family member 1B1", "SLCO1B3", "HBLRR", "LST-2", "LST-3TM13", "LST3", "OATP-8", "OATP1B3", "OATP8", "SLC21A8", "solute carrier organic anion transporter family member 1B3"]}
-{"question": "Gene Noonan syndrome has a genetic association with diseases such as", "references": ["PTPN11", "BPTP3", "CFC", "JMML", "METCDS", "NS1", "PTP-1D", "PTP2C", "SH-PTP2", "SH-PTP3", "SHP2", "protein tyrosine phosphatase, non-receptor type 11", "protein tyrosine phosphatase non-receptor type 11", "A2ML1", "CPAMD9", "alpha-2-macroglobulin like 1", "p170", "OMS"]}
-{"question": "Gene X-linked adrenoleukodystrophy has a genetic association with diseases such as", "references": ["PEX5", "PEX5", "PBD2A", "PBD2B", "PTS1-BP", "PTS1R", "PXR1", "RCDP5", "peroxisomal biogenesis factor 5", "ABCD1", "ABC42", "ALD", "ALDP", "AMN", "ATP binding cassette subfamily D member 1"]}
-{"question": "Gene syndactyly has a genetic association with diseases such as", "references": ["HOXD13", "BDE", "BDSD", "HOX4I", "SPD", "SPD1", "homeobox D13", "LMBR1", "ACHP", "C7orf2", "DIF14", "PPD2", "TPT", "ZRS", "LSS", "THYP", "limb development membrane protein 1", "GJA1", "AVSD3", "CMDR", "CX43", "EKVP", "GJAL", "HLHS1", "HSS", "ODDD", "PPKCA", "gap junction protein alpha 1", "EKVP3"]}
-{"question": "Gene Krabbe disease has a genetic association with diseases such as", "references": ["PSAP", "GLBA", "SAP1", "prosaposin", "SAP2", "PSAPD", "PARK24"]}
-{"question": "Gene transmissible spongiform encephalopathy has a genetic association with diseases such as", "references": ["PRNP", "ASCR", "AltPrP", "CD230", "CJD", "GSS", "KURU", "PRIP", "PrP", "PrP27-30", "PrP33-35C", "PrPc", "p27-30", "prion protein", "SEMA3A", "COLL1", "HH16", "Hsema-I", "Hsema-III", "SEMA1", "SEMAD", "SEMAIII", "SEMAL", "SemD", "coll-1", "semaphorin 3A"]}
-{"question": "Gene metachromatic leukodystrophy has a genetic association with diseases such as", "references": ["PSAP", "GLBA", "SAP1", "prosaposin", "SAP2", "PSAPD", "PARK24"]}
-{"question": "Gene Brown-Vialetto-Van Laere syndrome has a genetic association with diseases such as", "references": ["SLC52A3", "BVVLS", "BVVLS1", "C20orf54", "RFT2", "RFVT3", "bA371L19.1", "hRFT2", "solute carrier family 52 member 3"]}
-{"question": "Gene PRKCB has a genetic association with diseases such as", "references": ["inflammatory bowel diseases", "IBD", "inflammatory bowel disease"]}
-{"question": "Gene HIV/AIDS has a genetic association with diseases such as", "references": ["PARD3B", "ALS2CR19", "PAR3B", "PAR3L", "PAR3LC", "PAR3beta", "Par3Lb", "par-3 family cell polarity regulator beta", "RXRG", "NR2B3", "RXRC", "Retinoid X receptor gamma"]}
-{"question": "Gene diabetes insipidus has a genetic association with diseases such as", "references": ["AVPR2", "ADHR", "DI1", "DIR", "DIR3", "NDI", "V2R", "arginine vasopressin receptor 2", "NDI1", "AQP2", "AQP-CD", "WCH-CD", "aquaporin 2", "NDI2"]}
-{"question": "Gene benign familial neonatal epilepsy has a genetic association with diseases such as", "references": ["KCNQ3", "BFNC2", "EBN2", "KV7.3", "potassium voltage-gated channel subfamily Q member 3", "KCNQ2", "BFNC", "BFNS1", "EBN", "EBN1", "EIEE7", "ENB1", "HNSPC", "KCNA11", "KV7.2", "KVEBN1", "potassium voltage-gated channel subfamily Q member 2", "DEE7"]}
-{"question": "Gene DCP1B has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene ADAMTS3 has a genetic association with diseases such as", "references": ["dental caries", "dental caries extending into pulp", "dental caries of smooth surface", "dental caries pit and fissure", "tooth decay", "cavities", "caries"]}
-{"question": "Gene MALT1 has a genetic association with diseases such as", "references": ["multiple sclerosis", "MS", "encephalomyelitis disseminata", "insular sclerosis", "disseminated sclerosis", "generalized multiple sclerosis", "Generalized multiple sclerosis (disorder)", "generalised multiple sclerosis", "Multiple sclerosis; MS", "Multiple sclerosis"]}
-{"question": "Gene RUNX1 has a genetic association with diseases such as", "references": ["smallpox", "ordinary smallpox", "variola", "variola vera", "esophageal cancer", "esophagus cancer", "oesophageal cancer", "cancer of the oesophagus", "malignant neoplasm of proximal third of esophagus", "malignant tumor of Proximal Third of esophagus", "Ca middle third oesophagus", "malignant neoplasm of distal third of esophagus", "malignant neoplasm of lower third of oesophagus", "Ca lower third oesophagus", "malignant tumor of the middle Third of the esophagus", "malignant neoplasm of upper third esophagus", "malignant tumor of abdominal esophagus", "malignant neoplasm of middle third of oesophagus", "malignant tumor of Distal Third of esophagus", "Malignant Neoplasm of the Abdominal Esophagus", "Malignant Tumor of the Abdominal Esophagus", "cancer of abdominal part of esophagus", "abdominal part of esophagus cancer", "malignant abdominal part of esophagus neoplasm", "malignant neoplasm of abdominal part of esophagus"]}
-{"question": "Gene BCS1L has a genetic association with diseases such as", "references": ["GRACILE syndrome", "Fellman disease", "Growth restriction-aminoaciduria-cholestasis-iron overload-lactic acidosis-early death syndrome", "Finnish Lethal Neonatal Metabolic Syndrome", "Growth delay-aminoaciduria-cholestasis-iron overload-lactic acidosis-early death syndrome", "Fellman Syndrome", "Lactic Acidosis, Finnish, With Hepatic Hemosiderosis", "GRACILE SYNDROME", "Growth Retardation, Amino Aciduria, Cholestasis, Iron Overload, Lactic Acidosis, and Early Death", "Bjornstad syndrome", "BJORNSTAD SYNDROME; BJS", "Pili Torti and Nerve Deafness", "BJS", "BJORNSTAD SYNDROME", "Deafness-pili torti-hypogonadism syndrome", "Ptd", "Bj\u00f6rnstad syndrome", "PTND", "Pili torti-sensorineural hearing loss", "Deafness and pili torti, Bjornstad type"]}
-{"question": "Gene tetra-amelia has a genetic association with diseases such as", "references": ["WNT3", "INT4", "TETAMS", "Wnt family member 3"]}
-{"question": "Gene MODY 6 has a genetic association with diseases such as", "references": ["NEUROD1", "BETA2", "BHF-1", "MODY6", "NEUROD", "bHLHa3", "neuronal differentiation 1", "T2D"]}
-{"question": "Gene sialuria has a genetic association with diseases such as", "references": ["GNE", "DMRV", "GLCNE", "IBM2", "NM", "Uae1", "glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase"]}
-{"question": "Gene DYNC2H1 has a genetic association with diseases such as", "references": ["tuberculosis", "hydrothorax", "Tuberculosis", "In the clinic. Tuberculosis", "TB", "phthisis", "phthisis pulmonalis", "consumption", "phtisis"]}
-{"question": "Gene familial partial lipodystrophy has a genetic association with diseases such as", "references": ["PPARG", "CIMT1", "GLM1", "NR1C3", "PPARG1", "PPARG2", "PPARgamma", "peroxisome proliferator activated receptor gamma", "PPARG5"]}
-{"question": "Gene atherosclerosis has a genetic association with diseases such as", "references": ["RYR3", "RYR-3", "ryanodine receptor 3", "ABI2", "ABI-2", "ABI2B", "AIP-1", "AblBP3", "SSH3BP2", "argBP1", "argBPIA", "argBPIB", "abl-interactor 2", "abl interactor 2", "AIP1", "DNAH5", "CILD3", "DNAHC5", "HL1", "KTGNR", "PCD", "dynein axonemal heavy chain 5"]}
-{"question": "Gene Pretzel syndrome has a genetic association with diseases such as", "references": ["STRADA", "LYK5", "NY-BR-96", "PMSE", "STRAD", "Stlk", "STE20-related kinase adaptor alpha", "STRAD alpha", "STE20 related adaptor alpha"]}
-{"question": "Gene Zellweger spectrum disorder has a genetic association with diseases such as", "references": ["PEX1", "PBD1A", "PBD1B", "ZWS", "ZWS1", "HMLR1", "peroxisomal biogenesis factor 1", "PEX10", "NALD", "PBD6A", "PBD6B", "RNF69", "peroxisomal biogenesis factor 10", "PEX11B", "PEX11-BETA", "PEX14B", "peroxisomal biogenesis factor 11 beta", "PEX11beta", "PEX12", "PAF-3", "PBD3A", "peroxisomal biogenesis factor 12", "PEX13", "NALD", "PBD11A", "PBD11B", "ZWS", "peroxisomal biogenesis factor 13", "PEX14", "NAPP2", "PBD13A", "Pex14p", "dJ734G22.2", "peroxisomal biogenesis factor 14", "PEX16", "PBD8A", "PBD8B", "peroxisomal biogenesis factor 16", "PEX19", "D1S2223E", "HK33", "PBD12A", "PMP1", "PMPI", "PXF", "PXMP1", "peroxisomal biogenesis factor 19", "PEX2", "PAF1", "PBD5A", "PBD5B", "PMP3", "PMP35", "PXMP3", "RNF72", "ZWS3", "peroxisomal biogenesis factor 2", "PEX26", "PBD7A", "PBD7B", "PEX26M1T", "Pex26pM1T", "peroxisomal biogenesis factor 26", "PEX3", "PBD10A", "TRG18", "peroxisomal biogenesis factor 3", "PBD10B", "PEX5", "PEX5", "PBD2A", "PBD2B", "PTS1-BP", "PTS1R", "PXR1", "RCDP5", "peroxisomal biogenesis factor 5", "PEX6", "PAF-2", "PAF2", "PBD4A", "PDB4B", "PXAAA1", "HMLR2", "peroxisomal biogenesis factor 6"]}
-{"question": "Gene TGFB2 has a genetic association with diseases such as", "references": ["chronic obstructive pulmonary disease", "COPD", "chronic obstructive airway disease", "chronic obstructive airways disease NOS", "chronic obstructive lung disease", "chronic obstructive airways disease NOS disorder", "chronic obstructive lung disease disorder", "COLD", "COLD (chronic obstructive lung disease)", "Chronic Obstructive Pulmonary Disease, (COPD)", "Pulmonary Disease (COPD), Chronic Obstructive", "Obstructive Pulmonary Disease (COPD), Chronic", "Chronic Obstructive Airways Disease", "Disease (COPD), Chronic Obstructive", "Chronic Obstructive Pulmonary Disease (COPD)", "obstructive lung disease, chronic", "COPD, Chronic Obstructive Pulmonary Disease", "Pulmonary Disease, Chronic Obstructive"]}
-{"question": "Gene ADAMTS7 has a genetic association with diseases such as", "references": ["coronary artery disease", "CAD", "atherosclerotic heart disease", "coronary heart disease", "ischemic heart disease", "IHD", "atherosclerotic cardiovascular disease", "CHD (coronary heart disease)", "coronary arteriosclerosis", "CHD", "coronary artery arteriosclerosis (disease)", "atherosclerosis of coronary artery", "Coronary Atherosclerosis"]}
-{"question": "Gene MRTFA has a genetic association with diseases such as", "references": ["breast cancer", "malignant neoplasm of breast", "malignant tumor of the breast", "mammary cancer", "primary breast cancer", "breast disorder"]}
-{"question": "Gene MEPE has a genetic association with diseases such as", "references": ["cardiovascular disease", "CV disease", "cardiovascular system disease", "myocardiovascular system disease", "heart, respiratory, and blood vessel disease", "diseases of the circulatory system", "cardiovascular diseases", "disease of subdivision of hemolymphoid system", "CVD"]}
-{"question": "Gene craniosynostosis has a genetic association with diseases such as", "references": ["BBS9", "B1", "C18", "D1", "PTHB1", "Bardet-Biedl syndrome 9", "TCF12", "CRS3", "HEB", "HTF4", "HsT17266", "bHLHb20", "TCF-12", "transcription factor 12", "p64", "SKI", "SKI proto-oncogene", "SGS", "SKV", "ERF", "CRS4", "PE-2", "PE2", "ETS2 repressor factor", "CHYTS", "MSX2", "CRS2", "FPP", "HOX8", "MSH", "PFM", "PFM1", "Msh homeobox 2"]}
-{"question": "Gene BRWD1 has a genetic association with diseases such as", "references": ["bipolar disorder", "BP", "manic depression", "BPAD"]}
-{"question": "Gene PTPN22 has a genetic association with diseases such as", "references": ["type-1 diabetes", "IDDM", "insulin-dependent diabetes mellitus", "type I diabetes mellitus", "T1DM", "insulin dependent diabetes", "juvenile diabetes", "diabetes mellitus juvenile type", "DIABETES MELLITUS, INSULIN-DEPENDENT; IDDM", "Diabetes Mellitus, Type 1", "Diabetes Mellitus, Insulin-Dependent, 1", "DIABETES MELLITUS, INSULIN-DEPENDENT", "Juvenile-Onset Diabetes", "Insulin-Dependent Diabetes Mellitus 1", "diabetes (type 1)", "type 1 diabetes mellitus", "vitiligo", "el morenito ojos claros"]}
-{"question": "Gene amyotrophic lateral sclerosis has a genetic association with diseases such as", "references": ["ITGA9", "ALPHA-RLC", "ITGA4L", "RLC", "integrin subunit alpha 9", "TSPAN9", "NET-5", "NET5", "PP1057", "tetraspanin 9", "TFAP2A", "AP-2", "AP-2alpha", "AP2TF", "BOFS", "TFAP2", "transcription factor AP-2 alpha", "ATP2B2", "PMCA2", "PMCA2a", "PMCA2i", "ATPase plasma membrane Ca2+ transporting 2", "EPB41", "erythrocyte membrane protein band 4.1", "4.1R", "EL1", "HE", "LRRC8C", "AD158", "FAD158", "leucine-rich repeat containing 8 family member C", "leucine rich repeat containing 8 family member C", "leucine rich repeat containing 8 VRAC subunit C", "NFASC", "NF", "NRCAML", "neurofascin", "NEDCPMD", "SLC25A12", "AGC1", "ARALAR", "solute carrier family 25 member 12", "EIEE39", "DEE39", "ERBB4", "ALS19", "HER4", "p180erbB4", "erb-b2 receptor tyrosine kinase 4", "TRPM8", "LTRPC6", "TRPP8", "transient receptor potential cation channel subfamily M member 8", "trp-p8", "LTrpC-6", "KCNMB2", "potassium calcium-activated channel subfamily M regulatory beta subunit 2", "MASP1", "3MC1", "CRARF", "CRARF1", "MAP1", "MASP", "MASP3", "MAp44", "PRSS5", "RaRF", "mannan binding lectin serine peptidase 1", "Mannan-binding lectin serine protease 1", "MBL associated serine protease 1", "MASP-3", "MAP-1", "ANXA3", "ANX3", "annexin A3", "SYNPO2", "synaptopodin 2", "SYISL", "INPP4B", "inositol polyphosphate-4-phosphatase type II B", "LAMA2", "LAMM", "Laminin, alpha 2", "laminin subunit alpha 2", "MDC1A", "CALN1", "CABP8", "calneuron 1", "ANK3", "ANKYRIN-G", "MRT37", "ankyrin 3, node of Ranvier (ankyrin G)", "ankyrin 3", "RBM19", "RNA binding motif protein 19", "Mrd1", "OLFM4", "GC1", "GW112", "OLM4", "OlfD", "UNQ362", "bA209J19.1", "hGC-1", "hOLfD", "olfactomedin 4", "DACH1", "DACH", "dachshund family transcription factor 1", "ZFYVE26", "FYVE-CENT", "SPG15", "zinc finger FYVE-type containing 26", "RGS6", "GAP", "regulator of G-protein signaling 6", "regulator of G protein signaling 6", "HA117", "S914", "ABCC12", "MRP9", "ATP binding cassette subfamily C member 12", "NEDD4L", "NEDD4-2", "NEDD4.2", "RSP5", "hNEDD4-2", "neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase", "PVNH7", "NEDD4 like E3 ubiquitin protein ligase", "PROCR", "CCCA", "CCD41", "EPCR", "protein C receptor", "NFATC2", "NFAT1", "NFATP", "nuclear factor of activated T-cells 2", "nuclear factor of activated T cells 2", "CHODL", "C21orf68", "MT75", "PRED12", "chondrolectin", "HOXD10", "HOX4", "HOX4D", "HOX4E", "Hox-4.4", "homeobox D10", "MRAS", "M-RAs", "R-RAS3", "RRAS3", "muscle RAS oncogene homolog", "NS11", "UNC13A", "Munc13-1", "unc-13 homolog A (C. elegans)", "unc-13 homolog A", "CPNE4", "COPN4", "CPN4", "copine 4", "LAMA3", "BM600", "E170", "LAMNA", "LOCS", "lama3a", "Laminin, alpha 3", "laminin subunit alpha 3", "ST3GAL3", "EIEE15", "MRT12", "SIAT6", "ST3GALII", "ST3GalIII", "ST3N", "ST3 beta-galactoside alpha-2,3-sialyltransferase 3", "ST3Gal III", "DEE15", "PTPRF", "LAR", "BNAH2", "protein tyrosine phosphatase, receptor type F", "protein tyrosine phosphatase receptor type F", "ARAP2", "CENTD1", "PARX", "ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 2", "IFRD1", "PC4", "TIS7", "interferon related developmental regulator 1", "PCSK5", "PC5", "PC6", "PC6A", "SPC6", "proprotein convertase subtilisin/kexin type 5", "CNOT2", "CDC36", "NOT2", "NOT2H", "HSPC131", "CCR4-NOT transcription complex subunit 2", "IDNADFS", "ANKS1B", "AIDA", "AIDA-1", "ANKS2", "EB-1", "EB1", "cajalin-2", "ankyrin repeat and sterile alpha motif domain containing 1B", "NRXN3", "C14orf60", "neurexin 3", "NT5C1A", "CN-I", "CN-IA", "CN1", "CN1A", "CNI", "5'-nucleotidase, cytosolic IA", "SLC39A11", "C17orf26", "ZIP11", "solute carrier family 39 member 11", "ZIP-11", "ATXN1", "ATX1", "D6S504E", "SCA1", "ataxin 1", "CNTN4", "AXCAM", "BIG-2", "contactin 4", "KIFAP3", "FLA3", "KAP-1", "KAP-3", "KAP3", "SMAP", "Smg-GDS", "dJ190I16.1", "kinesin associated protein 3", "DPP6", "DPPX", "VF2", "MRD33", "DPL1", "dipeptidyl peptidase like 6", "ITPR2", "CFAP48", "IP3R2", "ANHD", "INSP3R2", "inositol 1,4,5-trisphosphate receptor type 2", "ZFP64", "ZNF338", "ZFP64 zinc finger protein", "NEK1", "NY-REN-55", "SRPS2", "SRPS2A", "SRTD6", "NIMA related kinase 1", "ALS24", "SQSTM1", "A170", "OSIL", "PDB3", "ZIP3", "p60", "p62", "p62B", "FTDALS3", "Sequestosome 1", "NADGP", "DMRV", "ANG", "ALS9", "HEL168", "RAA1", "RNASE4", "RNASE5", "angiogenin, ribonuclease, RNase A family, 5", "angiogenin", "TARDBP", "ALS10", "TDP-43", "TAR DNA binding protein", "TUBA4A", "H2-ALPHA", "TUBA1", "ALS22", "tubulin alpha 4a", "FIG4", "ALS11", "CMT4J", "KIAA0274", "SAC3", "YVS", "dJ249I4.1", "BTOP", "Fig4", "FIG4 phosphoinositide 5-phosphatase", "OPTN", "ALS12", "FIP2", "GLC1E", "HIP7", "HYPL", "NRP", "TFIIIA-INTP", "optineurin", "FUS", "ALS6", "ETM4", "FUS1", "HNRNPP2", "POMP75", "TLS", "FUS RNA binding protein", "altFUS", "SOD1", "ALS", "ALS1", "HEL-S-44", "IPOA", "SOD", "hSod1", "homodimer", "superoxide dismutase 1, soluble", "superoxide dismutase 1", "STAHP", "VCP", "ALS14", "HEL-220", "HEL-S-70", "IBMPFD", "IBMPFD1", "TERA", "p97", "Valosin-containing protein", "CMT2Y", "valosin containing protein", "CDC48", "FTDALS6", "HNRNPA1", "ALS19", "ALS20", "HNRPA1", "HNRPA1L3", "IBMPFD3", "hnRNP A1", "hnRNP-A1", "UP 1", "heterogeneous nuclear ribonucleoprotein A1", "PFN1", "ALS18", "Profilin 1", "UBQLN2", "ALS15", "CHAP1", "DSK2", "N4BP4", "PLIC2", "HRIHFB2157", "ubiquilin 2", "VAPB", "ALS8", "VAMP-B", "VAP-B", "VAMP (vesicle-associated membrane protein)-associated protein B and C", "VAMP associated protein B and C", "CHMP2B", "ALS17", "CHMP2.5", "DMT1", "VPS2-2", "VPS2B", "charged multivesicular body protein 2B", "FTDALS7"]}
-{"question": "Gene Hystrix-like ichthyosis\u2013deafness syndrome has a genetic association with diseases such as", "references": ["GJB2", "CX26", "DFNA3", "DFNA3A", "DFNB1", "DFNB1A", "HID", "KID", "NSRD1", "PPK", "gap junction protein beta 2", "BAPS"]}
-{"question": "Gene TCF3 has a genetic association with diseases such as", "references": ["Hodgkin lymphoma", "HL", "Hodgkin disease", "Hodgkin's sarcoma", "Hodgkins lymphoma", "stage I Subdiaphragmatic Hodgkin Lymphoma", "stage II Subdiaphragmatic Hodgkin Lymphoma", "Hodgkin's lymphoma; HL", "Hodgkin's disease", "Hodgkin's lymphoma"]}
-{"question": "Gene UBXN11 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene cannabis dependence has a genetic association with diseases such as", "references": ["UCHL5", "CGI-70", "INO80R", "UCH-L5", "UCH37", "Ubiquitin carboxyl-terminal hydrolase L5", "ubiquitin C-terminal hydrolase L5", "CHST11", "C4ST", "C4ST-1", "C4ST1", "HSA269537", "carbohydrate (chondroitin 4) sulfotransferase 11", "carbohydrate sulfotransferase 11", "OCBMD"]}
-{"question": "Gene POLD1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "MDP syndrome", "Mandibular hypoplasia-hearing loss-progeroid syndrome", "MDPL", "MDP syndrome", "MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME; MDPL", "MANDIBULAR HYPOPLASIA, DEAFNESS, PROGEROID FEATURES, AND LIPODYSTROPHY SYNDROME", "Polymerase proofreading-related adenomatous polyposis", "PPAP", "Polymerase proofreading-associated polyposis"]}
-{"question": "Gene mucosulfatidosis has a genetic association with diseases such as", "references": ["SUMF1", "AAPA3037", "FGE", "UNQ3037", "sulfatase modifying factor 1"]}
-{"question": "Gene EFNB1 has a genetic association with diseases such as", "references": ["Craniofrontonasal dysplasia", "CFNS", "Craniofrontonasal syndrome", "CFND", "Craniofrontonasal dysostosis"]}
-{"question": "Gene NAV2 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene CALM3 has a genetic association with diseases such as", "references": ["long QT syndrome", "long QT interval syndrome", "LQTS", "Romano-Ward syndrome (disorder)", "Romano-Ward syndrome", "LQT", "long Q-T syndrome", "Ventricular arrhythmia associated with long QT syndrome", "Romano Ward long QT syndrome"]}
-{"question": "Gene RPS6KA2 has a genetic association with diseases such as", "references": ["dental caries", "dental caries extending into pulp", "dental caries of smooth surface", "dental caries pit and fissure", "tooth decay", "cavities", "caries"]}
-{"question": "Gene TTPA has a genetic association with diseases such as", "references": ["familial isolated deficiency of vitamin E", "ataxia with isolated vitamin E deficiency", "familial isolated vitamin E deficiency", "Isolated vitamin E deficiency", "Friedreich-like ataxia", "AVED", "Ataxia with vitamin E deficiency", "familial isolated deficiency of vitamin type E", "VED", "VITAMIN E, FAMILIAL ISOLATED DEFICIENCY OF", "Ataxia, Friedreich-Like, With Selective Vitamin E Deficiency", "VITAMIN E, FAMILIAL ISOLATED DEFICIENCY OF; VED"]}
-{"question": "Gene PTPN11 has a genetic association with diseases such as", "references": ["juvenile myelomonocytic leukemia", "Juvenile Chronic Myeloid Leukemia", "Juvenile Myelomonocytic Leukemia", "Juvenile chronic myelomonocytic leukemia", "Chronic Myelomonocytic Leukemia", "JUVENILE MYELOMONOCYTIC LEUKEMIA; JMML", "Juvenile Chronic Myelogenous Leukemia", "JCML", "Leukemia, Chronic Myelomonocytic", "Leukemia, Juvenile Myelomonocytic", "JMML", "Metachondromatosis", "METACHONDROMATOSIS", "METACHONDROMATOSIS; METCDS", "METCDS", "metachondromatosis"]}
-{"question": "Gene CNTN4 has a genetic association with diseases such as", "references": ["amyotrophic lateral sclerosis", "ALS", "Lou Gehrig's disease", "motor neuron disease, bulbar", "Lou Gehrig disease", "Charcot disease", "Amyotrophic lateral sclerosis", "motor neurone disease", "Lou Gehrig's disease"]}
-{"question": "Gene CYP4V2 has a genetic association with diseases such as", "references": ["Bietti crystalline corneoretinal dystrophy", "Bietti's crystalline dystrophy", "BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY", "Bietti Crystalline Dystrophy", "BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY; BCD", "Bietti crystalline retinopathy", "Bietti Tapetoretinal Degeneration With Marginal Corneal Dystrophy", "BCD"]}
-{"question": "Gene progressive supranuclear palsy has a genetic association with diseases such as", "references": ["STX6", "syntaxin 6", "EIF2AK3", "PEK", "PERK", "WRS", "eukaryotic translation initiation factor 2 alpha kinase 3", "SLCO1A2", "OATP", "OATP-A", "OATP1A2", "SLC21A3", "solute carrier organic anion transporter family member 1A2", "IRF4", "LSIRF", "MUM1", "NF-EM5", "SHEP8", "interferon regulatory factor 4"]}
-{"question": "Gene FOXC2 has a genetic association with diseases such as", "references": ["Lymphedema\u2013distichiasis syndrome", "LYMPHEDEMA-DISTICHIASIS SYNDROME", "Lymphedema With Distichiasis", "Hereditary lymphedema-distichiasis syndrome (subtype)", "Lymphedema-Distichiasis Syndrome With Renal Disease and Diabetes Mellitus", "lymphedema-distichiasis syndrome"]}
-{"question": "Gene 3MC syndrome 1 has a genetic association with diseases such as", "references": ["MASP1", "3MC1", "CRARF", "CRARF1", "MAP1", "MASP", "MASP3", "MAp44", "PRSS5", "RaRF", "mannan binding lectin serine peptidase 1", "Mannan-binding lectin serine protease 1", "MBL associated serine protease 1", "MASP-3", "MAP-1"]}
-{"question": "Gene centronuclear myopathy has a genetic association with diseases such as", "references": ["SPEG", "APEG-1", "APEG1", "BPEG", "SPEGalpha", "SPEGbeta", "CNM5", "SPEG complex locus", "MYLK6", "striated muscle enriched protein kinase", "MYF6", "CNM3", "MRF4", "bHLHc4", "myf-6", "Myf6", "myogenic factor 6", "MTM1", "CNM", "MTMX", "XLMTM", "Myotubularin 1", "myotubularin", "DNM2", "CMT2M", "CMTDI1", "CMTDIB", "DI-CMTB", "DYN2", "DYNII", "LCCS5", "dynamin 2", "CCDC78", "C16orf25", "CNM4", "JFP10", "hsCCDC78", "Ccdc78", "coiled-coil domain containing 78", "BIN1", "AMPH2", "AMPHL", "SH3P9", "bridging integrator 1", "CNM2"]}
-{"question": "Gene HEXA has a genetic association with diseases such as", "references": ["Tay-Sachs disease", "hexosaminidase A deficiency", "Tay-Sachs disease (disorder)", "disease, Tay-Sachs", "GM2 gangliosidosis, type 1", "Hexosaminidase a Deficiency, Adult Type", "Hexosaminidase alpha-subunit deficiency (variant B)", "Gm2-Gangliosidosis, Variant B1", "Gm2-Gangliosidosis, Adult Chronic Type", "B variant GM2 gangliosidosis", "Gm2-Gangliosidosis, Type 1", "Hexa Deficiency", "GM2 gangliosidosis, B, B1 variant", "Sphingolipidosis, Tay-Sachs", "TAY-SACHS DISEASE; TSD", "TSD", "Tay-Sachs Disease, Variant B1", "Tay-Sachs Disease, Juvenile", "Tay-Sachs Disease, Pseudo-Ab Variant", "B Variant Gm2-Gangliosidosis", "TAY-SACHS DISEASE", "Gangliosidosis GM2 , type 1"]}
-{"question": "Gene SNTB1 has a genetic association with diseases such as", "references": ["myopia", "near-sightedness", "short-sightedness", "near vision"]}
-{"question": "Gene congenital disorder of glycosylation type IIc has a genetic association with diseases such as", "references": ["SLC35C1", "CDG2C", "FUCT1", "solute carrier family 35 member C1"]}
-{"question": "Gene Macrocephaly-capillary malformation has a genetic association with diseases such as", "references": ["PIK3CA", "CLOVE", "CWS5", "MCAP", "MCM", "MCMTC", "PI3K", "p110-alpha", "PI3K-alpha", "phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha", "CLAPO", "CCM4"]}
-{"question": "Gene Lenz microphthalmia syndrome has a genetic association with diseases such as", "references": ["NAA10", "ARD1", "ARD1A", "ARD1P", "DXS707", "MCOPS1", "NATD", "TE2", "OGDNS", "N(alpha)-acetyltransferase 10, NatA catalytic subunit", "hARD1", "N-alpha-acetyltransferase 10, NatA catalytic subunit"]}
-{"question": "Gene SMS has a genetic association with diseases such as", "references": ["Snyder-Robinson syndrome", "syndromic X-linked intellectual disability Snyder type", "SRS", "Snyder-Robinson mental retardation syndrome", "mental retardation, X-linked, Snyder-Robinson type", "spermine synthase deficiency", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE; MRXSSR", "X-linked intellectual disability, Snyder type", "MENTAL RETARDATION, X-LINKED, SYNDROMIC, SNYDER-ROBINSON TYPE", "MRXSSR"]}
-{"question": "Gene MAPK10 has a genetic association with diseases such as", "references": ["peripheral artery disease", "PAD", "peripheral obliterative arteriopathy", "peripheral arterial disease", "peripheral arterial disorder"]}
-{"question": "Gene LMAN2L has a genetic association with diseases such as", "references": ["bipolar disorder", "BP", "manic depression", "BPAD"]}
-{"question": "Gene ANKRD1 has a genetic association with diseases such as", "references": ["scimitar syndrome", "pulmonary venolobar syndrome", "total anomalous pulmonary venous return", "TOTAL ANOMALOUS PULMONARY VENOUS RETURN 1", "TOTAL ANOMALOUS PULMONARY VENOUS RETURN 1; TAPVR1", "TAPVR", "Anomalous Pulmonary Venous Return", "Scimitar Anomaly", "TAPVR1"]}
-{"question": "Gene BDP1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene PGM3 deficiency has a genetic association with diseases such as", "references": ["PGM3", "AGM1", "IMD23", "PAGM", "PGM 3", "Phosphoglucomutase 3"]}
-{"question": "Gene KCND3 has a genetic association with diseases such as", "references": ["smallpox", "ordinary smallpox", "variola", "variola vera"]}
-{"question": "Gene dysferlinopathy has a genetic association with diseases such as", "references": ["DYSF", "FER1L1", "LGMD2B", "MMD1", "dysferlin", "LGMDR2"]}
-{"question": "Gene ABCG5 has a genetic association with diseases such as", "references": ["sitosterolemia", "phytosterolemia", "SITOSTEROLEMIA", "Stsl", "Plant sterol storage disease", "Retention of dietary cholesterol and abnormal retention of non-cholesterol sterols in the body", "Macrothrombocytopenia/Stomatocytosis, Mediterranean"]}
-{"question": "Gene CHD7 has a genetic association with diseases such as", "references": ["CHARGE syndrome", "CHARGE association", "Coloboma-heart defects-atresia choanae-retardation of growth and development-genitourinary problems-ear abnormalities syndrome", "CHARGE SYNDROME", "Coloboma, Heart Defects, Choanal Atresia, Retardation of Growth and Development, Genital Abnormalities, and Ear Anomalies Association", "Hall-Hittner syndrome", "Coloboma, Heart Malformation, Choanal Atresia, Retardation of Growth and Development, Genital Abnormalities, and Ear Malformations (CHARGE) Association", "Charge Association--Coloboma, Heart Anomaly, Choanal Atresia, Retardation, Genital and Ear Anomalies"]}
-{"question": "Gene GATA4 has a genetic association with diseases such as", "references": ["myopia", "near-sightedness", "short-sightedness", "near vision", "tetralogy of Fallot", "Ventricular septal defect with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle", "TOF", "Fallot tetralogy", "TETRALOGY OF FALLOT", "TETRALOGY OF FALLOT; TOF"]}
-{"question": "Gene adult polyglucosan body disease has a genetic association with diseases such as", "references": ["GBE1", "APBD", "GBE", "GSD4", "glucan (1,4-alpha-), branching enzyme 1", "1,4-alpha-glucan branching enzyme 1"]}
-{"question": "Gene hepatitis C has a genetic association with diseases such as", "references": ["TSBP1", "TSBP", "chromosome 6 open reading frame 10", "testis expressed basic protein 1", "C6orf10", "BTNL2", "BTL-II", "BTN7", "HSBLMHC1", "SS2", "butyrophilin like 2", "RNF7", "CKBBP1", "ROC2", "SAG", "ring finger protein 7", "rbx2", "MERTK", "MER", "RP38", "c-mer", "Tyro12", "c-Eyk", "MER proto-oncogene, tyrosine kinase", "SLC22A3", "EMT", "EMTH", "OCT3", "solute carrier family 22 member 3", "DEPDC5", "DEP.5", "FFEVF", "DEP domain containing 5", "FFEVF1", "DEP domain containing 5, GATOR1 subcomplex subunit", "ITPA", "C20orf37", "HLC14-06-P", "dJ794I6.3", "My049", "ITPase", "NTPase", "inosine triphosphatase", "DEE35"]}
-{"question": "Gene PITX2 has a genetic association with diseases such as", "references": ["iridogoniodysgenesis syndrome", "IGDS", "IRID 1", "IRID 2", "iridogoniodysgenesis type 1", "iridogoniodysgenesis type 2", "Iridogoniodysgenesis Syndrome", "Iridogoniodysgenesis, Type 2", "Iris Hypoplasia With Early-Onset Glaucoma, Autosomal Dominant", "IRIDOGONIODYSGENESIS, TYPE 2; IRID2", "IRID2", "ASGD4", "ANTERIOR SEGMENT DYSGENESIS 4; ASGD4"]}
-{"question": "Gene scimitar syndrome has a genetic association with diseases such as", "references": ["ANKRD1", "ALRP", "C-193", "CARP", "CVARP", "MCARP", "bA320F15.2", "ankyrin repeat domain 1"]}
-{"question": "Gene glycoproteinosis has a genetic association with diseases such as", "references": ["NEU1", "NANH", "NEU", "SIAL1", "neuraminidase 1 (lysosomal sialidase)", "neuraminidase 1"]}
-{"question": "Gene PRM1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene ARHGAP26 has a genetic association with diseases such as", "references": ["juvenile myelomonocytic leukemia", "Juvenile Chronic Myeloid Leukemia", "Juvenile Myelomonocytic Leukemia", "Juvenile chronic myelomonocytic leukemia", "Chronic Myelomonocytic Leukemia", "JUVENILE MYELOMONOCYTIC LEUKEMIA; JMML", "Juvenile Chronic Myelogenous Leukemia", "JCML", "Leukemia, Chronic Myelomonocytic", "Leukemia, Juvenile Myelomonocytic", "JMML"]}
-{"question": "Gene CELF1 has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene Peutz-Jeghers syndrome has a genetic association with diseases such as", "references": ["STK11", "LKB1", "PJS", "hLKB1", "serine/threonine kinase 11"]}
-{"question": "Gene FDFT1 has a genetic association with diseases such as", "references": ["fatty liver disease", "hepatic lipidosis", "fatty degeneration of the liver", "steatosis of the liver", "Fatty liver disease", "fatty change of liver", "steatosis of liver (disorder)", "steatosis of liver", "liver steatosis", "hepatic steatosis", "fatty liver"]}
-{"question": "Gene BTBD9 has a genetic association with diseases such as", "references": ["restless legs syndrome", "WED", "Willis-Ekbom disease", "Wittmaack-Ekbom syndrome", "RLS", "Restless Leg Syndrome"]}
-{"question": "Gene Pelizaeus-Merzbacher disease has a genetic association with diseases such as", "references": ["PLP1", "GPM6C", "HLD1", "MMPL", "PLP", "PLP/DM20", "PMD", "SPG2", "proteolipid protein 1"]}
-{"question": "Gene multiple sclerosis has a genetic association with diseases such as", "references": ["BTNL2", "BTL-II", "BTN7", "HSBLMHC1", "SS2", "butyrophilin like 2", "HLA-DRA", "HLA-DRA1", "MLRW", "major histocompatibility complex, class II, DR alpha", "HACE1", "SPPRS", "HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1", "VTI1A", "MMDS3", "MVti1", "VTI1RP2", "Vti1-rp2", "vesicle transport through interaction with t-SNAREs 1A", "TLL1", "ASD6", "TLL", "tolloid like 1", "RNASEL", "PRCA1", "RNS4", "ribonuclease L", "TSBP1", "TSBP", "chromosome 6 open reading frame 10", "testis expressed basic protein 1", "C6orf10", "MLANA", "MART-1", "MART1", "melan-A", "STAT3", "ADMIO", "APRF", "HIES", "signal transducer and activator of transcription 3", "ADMIO1", "EPS15L1", "EPS15R", "epidermal growth factor receptor pathway substrate 15 like 1", "TAGAP", "ARHGAP47", "IDDM21", "TAGAP1", "FKSG15", "T-cell activation RhoGTPase activating protein", "T cell activation RhoGTPase activating protein", "ZMIZ1", "MIZ", "RAI17", "TRAFIP10", "ZIMP10", "hZIMP10", "zinc finger MIZ-type containing 1", "NEDDFSA", "AHI1", "AHI-1", "JBTS3", "ORF1", "dJ71N10.1", "Abelson helper integration site 1", "BACH2", "BTBD25", "BTB domain and CNC homolog 2", "IMD60", "BATF", "B-ATF", "BATF1", "SFA-2", "SFA2", "basic leucine zipper ATF-like transcription factor", "CHST12", "C4S-2", "C4ST-2", "C4ST2", "carbohydrate (chondroitin 4) sulfotransferase 12", "carbohydrate sulfotransferase 12", "CLEC16A", "Gop-1", "KIAA0350", "C-type lectin domain family 16 member A", "C-type lectin domain containing 16A", "DLEU1", "BCMS", "BCMS1", "DLB1", "DLEU2", "LEU1", "LEU2", "LINC00021", "NCRNA00021", "XTP6", "deleted in lymphocytic leukemia 1 (non-protein coding)", "deleted in lymphocytic leukemia 1", "EVI5", "NB4S", "EVI-5", "ecotropic viral integration site 5", "FCRL3", "CD307c", "FCRH3", "IFGP3", "IRTA3", "SPAP2", "Fc receptor like 3", "IL7R", "CD127", "CDW127", "IL-7R-alpha", "IL7RA", "ILRA", "Interleukin-7 receptor-\u03b1", "interleukin 7 receptor", "MALT1", "IMD12", "MLT", "MLT1", "PCASP1", "MALT1 paracaspase", "MAPK1", "ERK", "ERK-2", "ERK2", "ERT1", "MAPK2", "P42MAPK", "PRKM1", "PRKM2", "p38", "p40", "p41", "p41mapk", "p42-MAPK", "mitogen-activated protein kinase 1", "NS13", "MERTK", "MER", "RP38", "c-mer", "Tyro12", "c-Eyk", "MER proto-oncogene, tyrosine kinase", "MPV17L2", "FKSG24", "MPV17 mitochondrial inner membrane protein like 2", "NDFIP1", "N4WBP5", "Nedd4 family interacting protein 1", "PVR", "CD155", "HVED", "NECL5", "Necl-5", "PVS", "TAGE4", "poliovirus receptor", "PVR cell adhesion molecule", "RGS14", "regulator of G protein signaling 14", "RPS6KB1", "PS6K", "S6K", "S6K-beta-1", "S6K1", "STK14A", "p70 S6KA", "p70(S6K)-alpha", "p70-S6K", "p70-alpha", "P70-S6 Kinase 1", "ribosomal protein S6 kinase B1", "p70S6K", "p70S6 kinase", "RREB1", "FINB", "HNT", "LZ321", "RREB-1", "Zep-1", "ras responsive element binding protein 1", "SAE1", "AOS1", "HSPC140", "SUA1", "UBLE1A", "SUMO1 activating enzyme subunit 1", "SP140", "LYSP100", "LYSP100-A", "LYSP100-B", "SP140 nuclear body protein", "TNFSF14", "CD258", "HVEML", "LIGHT", "LTg", "TR2", "TNLG1D", "tumor necrosis factor superfamily member 14", "TNF superfamily member 14", "ZFP36L1", "BRF1", "Berg36", "ERF-1", "ERF1", "RNF162B", "TIS11B", "cMG1", "ZFP36 ring finger protein-like 1", "ZFP36 ring finger protein like 1", "YWHAG", "14-3-3GAMMA", "PPP1R170", "tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein gamma", "EIEE56", "DEE56", "SUMF1", "AAPA3037", "FGE", "UNQ3037", "sulfatase modifying factor 1", "CUEDC1", "CUE domain containing 1", "VAV2", "VAV-2", "vav guanine nucleotide exchange factor 2", "CBLB", "Cbl-b", "RNF56", "Nbla00127", "Cbl proto-oncogene B", "MGAT5", "GNT-V", "GNT-VA", "mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase", "alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase", "MGAT5A", "glcNAc-T V", "CSMD1", "PPP1R24", "CUB and Sushi multiple domains 1", "GPC5", "glypican 5", "NLRP11", "CLR19.6", "NALP11", "NOD17", "PAN10", "PYPAF6", "PYPAF7", "NLR family, pyrin domain containing 11", "NLR family pyrin domain containing 11", "C1GALT1", "C1GALT", "T-synthase", "core 1 synthase, glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase 1"]}
-{"question": "Gene KRT2 has a genetic association with diseases such as", "references": ["ichthyosis bullosa of Siemens", "superficial epidermolytic ichthyosis", "bullous type ichthyosis", "Ichthyosis, Bullous Type", "ICHTHYOSIS BULLOSA OF SIEMENS; IBS", "ICHTHYOSIS BULLOSA OF SIEMENS", "IBS", "Bullous type of ichthyosis", "Ichthyosis Exfoliativa", "SEI"]}
-{"question": "Gene PICALM has a genetic association with diseases such as", "references": ["Alzheimer's disease", "Alzheimer", "Alzheimers", "AD", "Alzheimer disease", "Alzheimer's dementia", "Alzheimers dementia", "Alzheimer disease, familial", "Alzheimer dementia", "Alzheimer's Disease", "Alzheimers disease"]}
-{"question": "Gene hereditary neuropathy with liability to pressure palsies has a genetic association with diseases such as", "references": ["PMP22", "CMT1A", "CMT1E", "DSS", "GAS-3", "HMSNIA", "HNPP", "Sujojp110", "GAS3", "peripheral myelin protein 22", "CIDP", "Sp110"]}
-{"question": "Gene SCRN1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene DCAF17 has a genetic association with diseases such as", "references": ["Woodhouse\u2013Sakati syndrome", "Woodhouse-Sakati syndrome", "Hypogonadism, diabetes mellitus, alopecia, mental retardation, and electrocardiographic abnormalities", "Woodhouse Sakati syndrome", "WOODHOUSE-SAKATI SYNDROME", "Diabetes-hypogonadism-deafness-intellectual disability syndrome", "Extrapyramidal Disorder, Progressive, With Primary Hypogonadism, Mental Retardation, and Alopecia", "Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, Deafness, and Extrapyramidal Syndrome"]}
-{"question": "Gene Nicolaides\u2013Baraitser syndrome has a genetic association with diseases such as", "references": ["SMARCA2", "BAF190", "BRM", "NCBRS", "SNF2", "SNF2L2", "SNF2LA", "SWI2", "Sth1p", "hBRM", "hSNF2a", "SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2", "BIS"]}
-{"question": "Gene SYT6 has a genetic association with diseases such as", "references": ["breast cancer", "malignant neoplasm of breast", "malignant tumor of the breast", "mammary cancer", "primary breast cancer", "breast disorder"]}
-{"question": "Gene Micromastia has a genetic association with diseases such as", "references": ["PTPRF", "LAR", "BNAH2", "protein tyrosine phosphatase, receptor type F", "protein tyrosine phosphatase receptor type F"]}
-{"question": "Gene mammary Paget's disease has a genetic association with diseases such as", "references": ["NUP205", "C7orf14", "NPHS13", "nucleoporin 205kDa", "nucleoporin 205", "OPTN", "ALS12", "FIP2", "GLC1E", "HIP7", "HYPL", "NRP", "TFIIIA-INTP", "optineurin", "PML", "MYL", "PP8675", "RNF71", "TRIM19", "Promyelocytic leukemia protein", "promyelocytic leukemia", "Probable transcription factor PML", "PML nuclear body scaffold"]}
-{"question": "Gene PLCE1 has a genetic association with diseases such as", "references": ["arterial hypertension", "high blood pressure", "\"the silent killer\"", "hypertension", "chronic obstructive pulmonary disease", "COPD", "chronic obstructive airway disease", "chronic obstructive airways disease NOS", "chronic obstructive lung disease", "chronic obstructive airways disease NOS disorder", "chronic obstructive lung disease disorder", "COLD", "COLD (chronic obstructive lung disease)", "Chronic Obstructive Pulmonary Disease, (COPD)", "Pulmonary Disease (COPD), Chronic Obstructive", "Obstructive Pulmonary Disease (COPD), Chronic", "Chronic Obstructive Airways Disease", "Disease (COPD), Chronic Obstructive", "Chronic Obstructive Pulmonary Disease (COPD)", "obstructive lung disease, chronic", "COPD, Chronic Obstructive Pulmonary Disease", "Pulmonary Disease, Chronic Obstructive", "esophageal cancer", "esophagus cancer", "oesophageal cancer", "cancer of the oesophagus", "malignant neoplasm of proximal third of esophagus", "malignant tumor of Proximal Third of esophagus", "Ca middle third oesophagus", "malignant neoplasm of distal third of esophagus", "malignant neoplasm of lower third of oesophagus", "Ca lower third oesophagus", "malignant tumor of the middle Third of the esophagus", "malignant neoplasm of upper third esophagus", "malignant tumor of abdominal esophagus", "malignant neoplasm of middle third of oesophagus", "malignant tumor of Distal Third of esophagus", "Malignant Neoplasm of the Abdominal Esophagus", "Malignant Tumor of the Abdominal Esophagus", "cancer of abdominal part of esophagus", "abdominal part of esophagus cancer", "malignant abdominal part of esophagus neoplasm", "malignant neoplasm of abdominal part of esophagus"]}
-{"question": "Gene OCRL has a genetic association with diseases such as", "references": ["oculocerebrorenal syndrome", "LOWE OCULOCEREBRORENAL SYNDROME", "Lowe syndrome (disorder)", "oculocerebrorenal syndrome of Lowe", "Lowe syndrome", "Oculo-cerebro-renal syndrome", "Oculocerebrorenal dystrophy", "Phosphatidylinositol 4,5-biphosphate 5-phosphatase deficiency", "Lowe oculo-cerebro-renal syndrome", "OCR", "Oculo-cerebro-renal dystrophy", "Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency", "OCRL", "Ocrl1", "LOWE OCULOCEREBRORENAL SYNDROME; OCRL", "Lowe disease", "Dent disease", "Low-molecular-weight proteinuria with hypercalciuria and nephrocalcinosis", "Renal Fanconi syndrome with nephrocalcinosis and renal stones", "X-linked recessive hypercalciuric hypophosphatemic rickets", "X-linked recessive nephrolithiasis", "Dent disease 1", "Dent disease 2", "Dent's disease", "Nephrolithiasis type 2", "Dent Disease type 2"]}
-{"question": "Gene Diamond-Blackfan anemia has a genetic association with diseases such as", "references": ["RPL15", "DBA12", "EC45", "L15", "RPL10", "RPLY10", "RPYL10", "ribosomal protein L15", "RPL26", "DBA11", "L26", "ribosomal protein L26", "RPS29", "DBA13", "S29", "ribosomal protein S29", "uS14", "RPS26", "DBA10", "S26", "ribosomal protein S26", "eS26", "RPS10", "DBA9", "S10", "ribosomal protein S10", "RPS19", "DBA", "DBA1", "S19", "Ribosomal protein S19", "eS19", "LOH19CR1", "RPS7", "DBA8", "S7", "ribosomal protein S7", "eS7", "RPL11", "DBA7", "GIG34", "L11", "ribosomal protein L11", "uL5", "RPL5", "DBA6", "L5", "PPP1R135", "MSTP030", "Ribosomal protein L5", "uL18", "RPL35A", "DBA5", "L35A", "ribosomal protein L35a", "eL33", "RPS24", "DBA3", "S24", "ribosomal protein S24", "eS24", "RPS17", "DBA4", "RPS17L", "RPS17L1", "RPS17L2", "S17", "ribosomal protein S17"]}
-{"question": "Gene MNX1 has a genetic association with diseases such as", "references": ["Currarino syndrome", "Sacral Agenesis, Hereditary, With Presacral Mass, Anterior Meningocele, And/Or Teratoma, and Anorectal Malformation", "Currarino syndrome", "Scra1", "Sacral Agenesis Syndrome", "Currarino Triad"]}
-{"question": "Gene PKD2L1 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene RBBP6 has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese"]}
-{"question": "Gene SEMA3A has a genetic association with diseases such as", "references": ["obesity", "corpulence", "overfatness", "fatness", "obese", "transmissible spongiform encephalopathy", "TSE", "Prion disease pathway", "Prion protein disease", "Spongiform Encephalopathy", "prion induced disorder", "human prion disease", "Transmissible spongiform encephalopathy", "Prion disease", "prion diseases", "attention deficit hyperactivity disorder", "ADHD", "hyperkinetic disorder", "attention deficit disorder", "AD/HD", "A.D.H.D", "attention deficit/hyperactivity disorder", "attention deficit hyperactivity syndrome", "Attention Deficit Disorder with Hyperactivity", "ADDH"]}
-{"question": "Gene Properdin deficiency has a genetic association with diseases such as", "references": ["CFP", "BFD", "PFC", "PFD", "PROPERDIN", "complement factor properdin", "properdin"]}
-{"question": "Gene PHF8 has a genetic association with diseases such as", "references": ["bipolar disorder", "BP", "manic depression", "BPAD", "schizophrenia", "Morel-Kraepelin disease", "Kraepelin-Morel disease", "dementia pr\u00e6cox", "dementia praecox", "schizophrenia-1"]}
-{"question": "Gene Angelman syndrome has a genetic association with diseases such as", "references": ["UBE3A", "ANCR", "AS", "E6-AP", "EPVE6AP", "HPVE6A", "ubiquitin protein ligase E3A", "MECP2", "AUTSX3", "MRX16", "MRX79", "MRXS13", "MRXSL", "PPMX", "RS", "RTS", "RTT", "methyl-CpG binding protein 2"]}
-{"question": "Gene permanent neonatal diabetes mellitus has a genetic association with diseases such as", "references": ["ABCC8", "ABC36", "HHF1", "HI", "HRINS", "MRP8", "PHHI", "SUR", "SUR1", "SUR1delta2", "TNDM2", "ATP binding cassette subfamily C member 8", "PNDM3", "INS", "IDDM", "IDDM1", "IDDM2", "ILPR", "IRDN", "MODY10", "insulin", "PNDM4", "\u30a4\u30f3\u30b7\u30e5\u30ea\u30f3", "KCNJ11", "BIR", "HHF2", "IKATP", "KIR6.2", "MODY13", "PHHI", "TNDM3", "potassium voltage-gated channel subfamily J member 11", "potassium inwardly rectifying channel subfamily J member 11", "PNDM2"]}
-{"question": "Gene vitelliform macular dystrophy has a genetic association with diseases such as", "references": ["IMPG1", "GP147", "IPM150", "SPACR", "VMD4", "interphotoreceptor matrix proteoglycan 1", "RP91", "PRPH2", "AOFMD", "AVMD", "CACD2", "DS", "PRPH", "RDS", "RP7", "TSPAN22", "rd2", "MDBS1", "Peripherin 2", "peripherin 2 (retinal degeneration, slow)", "BEST1", "ARB", "BEST", "BMD", "RP50", "TU15B", "VMD2", "Bestrophin 1", "Best1V1Delta2"]}
-{"question": "Gene aniridia has a genetic association with diseases such as", "references": ["PAX6", "AN", "AN2", "D11S812E", "FVH1", "MGDA", "WAGR", "paired box 6", "ASGD5"]}
-{"question": "Gene pulmonary venoocclusive disease has a genetic association with diseases such as", "references": ["BMPR2", "BMPR-II", "BMPR3", "BMR2", "BRK-3", "POVD1", "PPH1", "T-ALK", "bone morphogenetic protein receptor type 2"]}
-{"question": "Gene DOOR syndrome has a genetic association with diseases such as", "references": ["TBC1D24", "DFNA65", "DFNB86", "DOORS", "EIEE16", "FIME", "TLDC6", "TBC1 domain family member 24", "EPRPDC", "DEE16"]}
-{"question": "Gene TSC22D1 has a genetic association with diseases such as", "references": ["vasculitis", "Angiitis", "Vasculitis Syndrome"]}
-{"question": "Gene isolated growth hormone deficiency has a genetic association with diseases such as", "references": ["GH1", "GH", "GH-N", "GHN", "IGHD1B", "hGH-N", "GHB5", "Growth hormone 1", "IGHD2", "IGHD1A", "SOX3", "GHDX", "MRGH", "PHP", "PHPX", "SOXB", "SRY-box 3", "SRY-box transcription factor 3"]}
-{"question": "Gene SGK1 has a genetic association with diseases such as", "references": ["smallpox", "ordinary smallpox", "variola", "variola vera"]}
-{"question": "Gene DNM1 has a genetic association with diseases such as", "references": ["attention deficit hyperactivity disorder", "ADHD", "hyperkinetic disorder", "attention deficit disorder", "AD/HD", "A.D.H.D", "attention deficit/hyperactivity disorder", "attention deficit hyperactivity syndrome", "Attention Deficit Disorder with Hyperactivity", "ADDH"]}
-{"question": "Gene Warsaw breakage syndrome has a genetic association with diseases such as", "references": ["DDX11", "CHL1", "CHLR1", "KRG2", "WABS", "DEAD/H-box helicase 11"]}
-{"question": "Gene spastic quadriplegia has a genetic association with diseases such as", "references": ["KANK1", "ANKRD15", "CPSQ2", "KANK", "KN motif and ankyrin repeat domains 1", "ADD3", "ADDL", "adducin 3", "CPSQ3", "GAD1", "CPSQ1", "GAD", "SCP", "glutamate decarboxylase 1", "DEE89"]}
-{"question": "Gene uncombable hair syndrome has a genetic association with diseases such as", "references": ["TCHH", "THH", "THL", "TRHY", "trichohyalin", "UHS3", "TGM3", "TGE", "transglutaminase 3", "UHS2"]}