An inherited metabolic disease that is has its basis in the disruption of branched-chain amino acid metabolic process.
Comprehensive, easy-to-understand information about this condition
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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