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Diseases
Genes (586)
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ATP7B
Wilson's Disease
TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
CBS
Classic Homocystinuria
FAM20A
Enamel-Renal Syndrome
AHDC1
Xia-Gibbs Syndrome
TGFBI
Granular Corneal Dystrophy Type I
DBH
Wilson's Disease
Dopamine Beta Hydroxylase Deficiency
IGF2
Bulimia Nervosa
Russell-Silver Syndrome
FGFR3
Collagenosis, Familial Reactive Perforating
Russell-Silver Syndrome
Epidermal Nevus Syndrome
IFIH1
Singleton Merten Syndrome
KRAS
Russell-Silver Syndrome
Epidermal Nevus Syndrome
H19
Russell-Silver Syndrome
NRAS
Epidermal Nevus Syndrome
ASS1
Citrullinemia Type I
ANXA5
Wilson's Disease
PRNP
Akinetic Mutism
Wilson's Disease
HTR2A
Bulimia Nervosa
Anorexia Nervosa
HMGA2
Russell-Silver Syndrome
PIK3CA
Russell-Silver Syndrome
Epidermal Nevus Syndrome