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Diseases
Genes (389)
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MYO5B
Microvillus Inclusion Disease
FMR1
Fragile X-Associated Tremor/ataxia Syndrome
RBM8A
Thrombocytopenia Absent Radius Syndrome
UROC1
Urocanase Deficiency
TTN
Cardiomyopathy, Dilated, 1m
STX3
Microvillus Inclusion Disease
CFH
Membranoproliferative Glomerulonephritis
TSLP
Membranoproliferative Glomerulonephritis
RBM20
Cardiomyopathy, Dilated, 1m
TNNT2
Cardiomyopathy, Dilated, 1m
SCN5A
Cardiomyopathy, Dilated, 1m
BAG3
Cardiomyopathy, Dilated, 1m
PRKACA
Fibrolamellar Hepatocellular Carcinoma
DNAJB1
Fibrolamellar Hepatocellular Carcinoma
MYH7
Cardiomyopathy, Dilated, 1m
MYBPC3
Cardiomyopathy, Dilated, 1m
MYH6
Cardiomyopathy, Dilated, 1m
SOST
Craniodiaphyseal Dysplasia
DMD
Cardiomyopathy, Dilated, 1m
PLN
Cardiomyopathy, Dilated, 1m