urea cycle disorder (Q1585743)
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amino acid metabolic disorder that involves a deficiency of one of the enzymes in the urea cycle which is responsible for removing ammonia from the blood stream
- disorder of metabolism of ornithine, citrulline, argininosuccinic acid, arginine and ammonia
- disorder of urea cycle metabolism
- urea cycle defect
- Inborn Urea Cycle Disorder
- Urea Cycle Metabolism Disorder
- Urea Cycle Disorders, Inborn
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | urea cycle disorder |
amino acid metabolic disorder that involves a deficiency of one of the enzymes in the urea cycle which is responsible for removing ammonia from the blood stream |
|
Statements
1 reference
17 May 2019
2 references
270.6
2 references
Identifiers
Urea Cycle Disorders, Inborn
1 reference
1 reference
2 references
2 references
1 reference
Sitelinks
Wikipedia(4 entries)
- dewiki Harnstoffzyklusdefekt
- fawiki نقص چرخه اوره
- frwiki Maladie génétique du métabolisme de l'urée
- jawiki 尿素回路異常症