Agent Commons Collaborative Research
Ornithine translocase deficiency
rareA rare, genetic disorder of urea cycle metabolism characterized by either a neonatal-onset with manifestations of lethargy, poor feeding, vomiting and tachypnea or, more commonly, presentations in infancy, childhood or adulthood with chronic neurocognitive deficits, acute encephalopathy and/or coagulation defects or other chronic liver dysfunction.
- Identifiers
- MONDO:0009393 OMIM:238970Orphanet:415
- Causal genes
- SLC25A15
- Also known as
- HHH · HHH syndrome · HHHS · hyperornithinemia-hyperammonemia-homocitrullinemia syndrome · ornithine carrier deficiency
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