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. http://en.wikipedia.org/wiki/Ornithine_translocase_deficiency
References
Ontology
Human Disease   ( DOID:0050720 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
Your Input Welcome
We welcome your input and comments. Please use this form to recommend updates to the information in ZFIN. We appreciate as much detail as possible and references as appropriate. We will review your comments promptly.
Please check the highlighted fields and try again.
Thank you for submitting comments. Your input has been emailed to ZFIN curators who may contact you if additional information is required.
Oops. Something went wrong. Please try again later.