ornithine translocase deficiency (Q7103627)
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 |
|---|---|---|---|
| default for all languages | No label defined |
||
| 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
1 reference
1 reference
6 references
1 reference
23 October 2026
1 reference
23 October 2026
0.9±0.1
1 reference
23 October 2026
0.55±0.25
1 reference
23 October 2026
0.55±0.25
1 reference
23 October 2026
0.55±0.25
1 reference
23 October 2026
0.55±0.25
1 reference
23 October 2026
0.17±0.12
1 reference
23 October 2026
0.17±0.12
1 reference
23 October 2026
1 reference
23 October 2026
1 reference
Identifiers
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
Sitelinks
Wikipedia(7 entries)
- dewiki HHH-Syndrom
- enwiki Ornithine translocase deficiency
- fawiki سندرم HHH
- fiwiki HHH-oireyhtymä
- jawiki 高オルニチン血症・高アンモニア血症・ホモシトルリン尿症症候群
- kowiki 오르니틴 트랜스로케이스 결핍
- zhwiki 高鳥胺酸血症-高氨血症-高瓜胺酸血症候群