OBO ID: DOID:0050720
Term Name: ornithine translocase deficiency Search Ontology:
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 ornithine translocase deficiency PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
SLC25A15 Hyperornithinemia-hyperammonemia-homocitrullinemia syndrome 238970
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None
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