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Last uploaded:
September 25, 2013
| Id | http://purl.bioontology.org/ontology/CSP/1849-1633
http://purl.bioontology.org/ontology/CSP/1849-1633
|
|---|---|
| Preferred Name | alpha 1 antitrypsin deficiency |
| Definitions |
autosomal recessive trait leading to destruction of lung tissue by neutrophil elastase and eventual emphysema; second only to cystic fibrosis as most common lethal genetic disorder among Caucasians of northern European ancestry.
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| definition | autosomal recessive trait leading to destruction of lung tissue by neutrophil elastase and eventual emphysema; second only to cystic fibrosis as most common lethal genetic disorder among Caucasians of northern European ancestry. |
|---|---|
| prefLabel | alpha 1 antitrypsin deficiency
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| Inverse of RO | |
| type | |
| tui | T047
|
| notation | 1849-1633
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| Semantic type UMLS property | |
| DID | 1849-1633
|
| cui | C0221757
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| Inverse of RB | |
| subClassOf |
| Delete | Subject | Author | Type | Created |
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| No notes to display |