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Diseases
Genes (693)
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MYO15A
Deafness, Autosomal Recessive 3
TTPA
Familial Isolated Vitamin E Deficiency
AGL
Glycogen Storage Disease Type Iii
ATP7B
Wilson's Disease
PIK3CD
Activated Pi3k Delta Syndrome
PQBP1
Renpenning's Syndrome
PHKG2
Glycogen Storage Disease Type Ix
Phosphorylase Kinase Deficiency
Glycogen Storage Disease Ixc
FAM20A
Enamel-Renal Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
IFIH1
Singleton Merten Syndrome
TNF
Myotonic Dystrophy
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Pleural Effusion
Wilson's Disease
DMPK
Myotonic Dystrophy
ASS1
Citrullinemia Type I
GRIN2A
Rolandic Epilepsy
PDGFB
Primary Familial Brain Calcification
ANXA5
Wilson's Disease
CTNS
Cystinosis
PHKA2
Glycogen Storage Disease Type Ix
Phosphorylase Kinase Deficiency
Glycogen Storage Disease Ixc
IL6
Myotonic Dystrophy
Familial Isolated Vitamin E Deficiency
Pleural Effusion
Wilson's Disease