Conditions / Genetic
urea cycle disorder
info · Genetic · ICD-10: E72.2
An amino acid metabolic disorder that involves a deficiency of one of the enzymes in the urea cycle which is responsible for removing ammonia from the blood stream.
Also known as: disorder of metabolism of ornithine, citrulline, argininosuccinic acid, arginine and ammonia; disorder of urea cycle metabolism; urea cycle defect