bn:03349329n
Noun Concept
Categories: Rare diseases, Autosomal recessive disorders, Amino acid metabolism disorders
EN
N-acetylglutamate synthase deficiency  Hyperammonemia Due to N-Acetylglutamate Synthetase Deficiency  N-acetyl glutamate synthetase deficiency  N-ACETYLGLUTAMATE SYNTHASE DEFICIENCY; NAGSD  N-Acetylglutamate Synthetase Deficiency
EN
N-Acetylglutamate synthase deficiency is an autosomal recessive urea cycle disorder. Wikipedia
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