ornithine translocase deficiency (Q7103627)
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amino acid metabolic disorder that has material basis in deficiency of ornithine translocase resulting in the accumulation of ammonia in the blood
- HHH syndrome
- Hyperornithinemia-Hyperammonemia-Homocitrullinuria (HHH) syndrome
- Ornithine translocase deficiency
- Ornithine carrier deficiency
- Triple H syndrome
- ORNT1 deficiency
- HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | ornithine translocase deficiency |
amino acid metabolic disorder that has material basis in deficiency of ornithine translocase resulting in the accumulation of ammonia in the blood |
|
Statements
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C129029
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Identifiers
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Sitelinks
Wikipedia(5 entries)
- dewiki HHH-Syndrom
- enwiki Ornithine translocase deficiency
- fawiki سندرم HHH
- fiwiki HHH-oireyhtymä
- zhwiki 高鳥胺酸血症-高氨血症-高瓜胺酸血症候群