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National Drug File - Reference Terminology
Last uploaded:
July 6, 2018
| Id | http://purl.bioontology.org/ontology/NDFRT/N0000181246
http://purl.bioontology.org/ontology/NDFRT/N0000181246
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|---|---|
| Preferred Name | Idiopathic Pulmonary Fibrosis [Disease/Finding] |
| Synonyms |
Idiopathic Pulmonary Fibrosis
Fibrocystic Pulmonary Dysplasia
Pulmonary Fibrosis, Idiopathic
Usual Interstitial Pneumonia
Idiopathic Pulmonary Fibrosis, Familial
Familial Idiopathic Pulmonary Fibrosis
Idiopathic Fibrosing Alveolitis, Chronic Form
Interstitial Pneumonitis, Usual
Fibrosing Alveolitis, Cryptogenic
Hamman-Rich Disease
Cryptogenic Fibrosing Alveolitis
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| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
Idiopathic Pulmonary Fibrosis
Fibrocystic Pulmonary Dysplasia
Pulmonary Fibrosis, Idiopathic
Usual Interstitial Pneumonia
Idiopathic Pulmonary Fibrosis, Familial
Familial Idiopathic Pulmonary Fibrosis
Idiopathic Fibrosing Alveolitis, Chronic Form
Interstitial Pneumonitis, Usual
Fibrosing Alveolitis, Cryptogenic
Hamman-Rich Disease
Cryptogenic Fibrosing Alveolitis
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See less
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|---|---|
| prefLabel | Idiopathic Pulmonary Fibrosis [Disease/Finding]
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| MESH DEFINITION | A common interstitial lung disease of unknown etiology, usually occurring between 50-70 years of age. Clinically, it is characterized by an insidious onset of breathlessness with exertion and a nonproductive cough, leading to progressive DYSPNEA. Pathological features show scant interstitial inflammation, patchy collagen fibrosis, prominent fibroblast proliferation foci, and microscopic honeycomb change.
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| MESH DUI | D054990
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| MESH UI | M0511887
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| MeSH name | Idiopathic Pulmonary Fibrosis
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| type | |
| tui | T047
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| May be treated by | |
| notation | N0000181246
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| Semantic type UMLS property | |
| NUI | N0000181246
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| cui | C1800706
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| NDFRT kind | DISEASE_KIND
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| subClassOf |
| Delete | Subject | Author | Type | Created |
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| No notes to display |