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Up to: Syndromic disease · Urea cycle disorder or inherited hyperammonemia
Ornithine translocase deficiency
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.
This condition has no sub-types.