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Ornithine carbamoyltransferase deficiency
rareOrnithine 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.
- Identifiers
- MONDO:0010703 OMIM:311250Orphanet:664
- Causal genes
- OTC
- Also known as
- OCT deficiency · ornithine carbamoyltransferase deficiency disease · ornithine transcarbamylase deficiency · OTC deficiency · OTCD
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