| Metadata | |
|---|---|
| ID | DOID:0050720 |
| Name | ornithine translocase deficiency |
| 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 |
| Xrefs | |
| Synonyms |
HHH syndrome [EXACT] Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) syndrome [EXACT] |
| Parent Relationships | |
| Subclass Logical Relationships |
has material basis in some ammonia |