Search Ontology:
Human Disease
ornithine translocase deficiency
- Term ID
- DOID:0050720
- Synonyms
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- 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. (2)
- References
- Ontology
- Human Disease ( DOID:0050720 )
- is a type of
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