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Last uploaded:
September 25, 2013
| Id | http://purl.bioontology.org/ontology/CSP/1849-9719
http://purl.bioontology.org/ontology/CSP/1849-9719
|
|---|---|
| Preferred Name | ornithinemia |
| Definitions |
excess of ornithine in the plasma, such as occurs in the genetic disorders gyrate atrophy of choroid and retina and hyperornithinemia-hyperamonemia-homocitrullinuria syndrome.
|
| Synonyms |
ornithine aminotransferase deficiency
gyrate atrophy of the retina
hyperornithinemia
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | excess of ornithine in the plasma, such as occurs in the genetic disorders gyrate atrophy of choroid and retina and hyperornithinemia-hyperamonemia-homocitrullinuria syndrome. |
|---|---|
| altLabel |
ornithine aminotransferase deficiency
gyrate atrophy of the retina
hyperornithinemia
|
| prefLabel | ornithinemia
|
| Inverse of RO | |
| type | |
| tui | T047
|
| notation | 1849-9719
|
| Semantic type UMLS property | |
| DID | 1849-9719
|
| cui |
C0599035
C0018425
|
| Inverse of RB | |
| subClassOf |
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |