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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
| Id | http://purl.bioontology.org/ontology/NDFRT/N0000000890
http://purl.bioontology.org/ontology/NDFRT/N0000000890
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|---|---|
| Preferred Name | Cystic Fibrosis [Disease/Finding] |
| Synonyms |
Cystic Fibrosis
Mucoviscidosis
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
Cystic Fibrosis
Mucoviscidosis
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|---|---|
| prefLabel | Cystic Fibrosis [Disease/Finding]
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| MESH DEFINITION | An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION.
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| MESH DUI | D003550
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| MESH UI | M0005551
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| MeSH name | Cystic Fibrosis
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| type | |
| tui | T047
|
| SNOMED CID | 190905008
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| May be treated by |
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| notation | N0000000890
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| Semantic type UMLS property | |
| NUI | N0000000890
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| cui | C0010674
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| NDFRT kind | DISEASE_KIND
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| subClassOf |
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| No notes to display |