A congenital disorder characterized by partial or complete absence of melanin pigment in the eyes, hair, or skin.
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disorder of methionine catabolism
MONDO:0000351
inborn serine deficiency
MONDO:0000421
cerebral creatine deficiency syndrome
MONDO:0000456
inborn organic aciduria
MONDO:0000688
gamma-amino butyric acid metabolism disorder
MONDO:0000698
homocystinuria
MONDO:0004737