Search Ontology:
Human Disease

ornithine translocase deficiency

Term ID
DOID:0050720
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. (2)
References
Ontology
Human Disease   ( DOID:0050720 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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