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Diseases
Genes (529)
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BAG3
Muscular Dystrophy, Selcen Type
Myopathy, Myofibrillar, 6
SERPINA1
Alpha-1-Antitrypsin Deficiency
Alpha-1 Antitrypsin Deficiency
Neutral Lipid Storage Disease
GHR
Laron Syndrome
FLNC
Myopathy, Myofibrillar, 5
ABHD5
Neutral Lipid Storage Disease
DES
Myofibrillar Myopathy
FBN1
Marfan Syndrome
KLHL40
Nemaline Myopathy 8
LMOD3
Nemaline Myopathy 10
LDB3
Myopathy, Myofibrillar, 4
Zaspopathy
Myofibrillar Myopathy
CSF1R
Hereditary Diffuse Leukoencephalopathy With Spheroids
PAX6
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, And Obesity Syndrome
WT1
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, And Obesity Syndrome
TNFAIP3
Haploinsufficiency Of A20
MYOT
Myopathy, Spheroid Body
PYROXD1
Myopathy, Myofibrillar, 8
COG4
Saul-Wilson Syndrome
POLA1
X-Linked Reticulate Pigmentary Disorder
MOCS1
Molybdenum Cofactor Deficiency
PRRT2
Paroxysmal Kinesigenic Choreoathetosis