An amino acid metabolic disorder characterized by impairment of the GABA catabolic pathway.
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
homocystinuria
MONDO:0004737
urea cycle disorder
MONDO:0004739