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Diseases
Genes (1164)
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SCN5A
Cardiac Conduction Defect
Cardiomyopathy, Dilated, 1i
DES
Myopathy, Myofibrillar, 1
Cardiomyopathy, Dilated, 1i
ABHD5
Cerebral Creatine Deficiency
ATP13A2
Kufor-Rakeb Syndrome
GAMT
Guanidinoacetate Methyltransferase Deficiency
PAH
Phenylketonuria (Pku)
GALE
Galactose Epimerase Deficiency
IFIH1
Singleton Merten Syndrome
NOTCH1
Melorheostosis
Erythroleukemia, Familial, Susceptibility To
Aortic Valve Disease 2
NKX2-5
Cardiac Conduction Defect
Aortic Valve Disease 2
Cardiomyopathy, Dilated, 1i
SLC39A8
Congenital Disorder Of Glycosylation, Type Iin
SMAD6
Aortic Valve Disease 2
TTN
Cardiomyopathy, Dilated, 1i
FREM1
Trigonocephaly
NDUFS2
Mitochondrial Complex I Deficiency, Nuclear Type 6
NUS1
Congenital Disorder Of Glycosylation, Type Iaa
KIAA1109
Alkuraya-Kucinskas Syndrome
CTNS
Cystinosis
DMD
Pectus Excavatum
Avascular Necrosis
Erythroleukemia, Familial, Susceptibility To
Phenylketonuria (Pku)
Decompression Illness
Cardiomyopathy, Dilated, 1i
LDB3
Myopathy, Myofibrillar, 1
Cardiomyopathy, Dilated, 1i