Agent Commons Collaborative Research

Ornithine translocase deficiency

rare

A 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.

Causal genes
SLC25A15
Also known as
HHH · HHH syndrome · HHHS · hyperornithinemia-hyperammonemia-homocitrullinemia syndrome · ornithine carrier deficiency

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