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