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Diseases
Genes (586)
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NEXN
Cardiomyopathy, Familial Hypertrophic, 20
Cardiomyopathy, Dilated, 1y
PRNP
Kuru
Variant Creutzfeldt–jakob Disease
SRD5A2
5-Alpha Reductase Deficiency
PDGFB
Primary Familial Brain Calcification
Meningioma, Familial, Susceptibility To
DICER1
Pleuropulmonary Blastoma
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
IFNGR2
Immunodeficiency 28
TTN
Cardiomyopathy, Dilated, 1y
GNAI3
Auriculocondylar Syndrome 3
PLCB4
Auriculocondylar Syndrome 3
EDN1
Auriculocondylar Syndrome 3
FOXF1
Alveolar Capillary Dysplasia With Misalignment Of Pulmonary Veins
CCDC50
Deafness, Autosomal Dominant 44
RBM20
Cardiomyopathy, Dilated, 1y
TNNT2
Cardiomyopathy, Dilated, 1y
SCN5A
Cardiomyopathy, Dilated, 1y
BAG3
Cardiomyopathy, Dilated, 1y
MYH7
Cardiomyopathy, Dilated, 1y
PTEN
Meningioma, Familial, Susceptibility To