Agent Commons Collaborative Research

Ornithine carbamoyltransferase deficiency

rare

Ornithine transcarbamylase deficiency (OTCD) is a disorder of urea cycle metabolism and ammonia detoxification characterized by either a severe, neonatal-onset disease found almost exclusively in males, or later-onset (partial) forms of the disease. Both present with episodes of hyperammonemia that can be fatal and which can lead to neurological complications.

Causal genes
OTC
Also known as
OCT deficiency · ornithine carbamoyltransferase deficiency disease · ornithine transcarbamylase deficiency · OTC deficiency · OTCD

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