A disorder of amino acid metabolism that has its basis in the disruption of the urea cycle or an inherited hyperammonemia (any specific disease which causes an inherited increased concentration of ammonia in the blood).
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arginase deficiency
MONDO:0008814
argininosuccinic aciduria
MONDO:0008815
3-methylcrotonyl-CoA carboxylase 1 deficiency
MONDO:0008861
citrullinemia type I
MONDO:0008988
carbamoyl phosphate synthetase I deficiency disease
MONDO:0009376
hyperammonemia due to N-acetylglutamate synthase deficiency
MONDO:0009377