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Acetohydroxamic Acid
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Acetohydroxamic Acid
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Amino Acid Metabolic Disorder
Aminoacidopathies
Argininosuccinic Aciduria
Carbamoyl Phosphate Synthetase I Deficiency, Hyperammonemia Due to
Central Nervous System Disease
Citrullinemia, Classic
Encephalopathy
Inborn Amino Acid Metabolism Disorder
Nephrolithiasis
Nephrolithiasis, Calcium Oxalate
Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to
Urea Cycle Disorder
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