Term Name:	ornithine translocase deficiency
Synonyms:	HHH syndrome, Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) syndrome
Definition:	An amino acid metabolic disorder that has_material_basis_in deficiency of ornithine translocase resulting in the accumulation of ammonia in the blood.
Ontology:	Human Disease [DOID:0050720]   ( DOID:0050720 )