Preferred Name | idiopathic pulmonary fibrosis | |
Synonyms |
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Definitions |
An idiopathic interstitial pneumonia which is a distinctive type of chronic fibrosing interstitial pneumonia with thick scarring in the lung creating a honeycomb appearance. The main symptoms start insidiously as shortness of breath on exertion, cough, and diminished stamina. Other common complaints include weight loss and fatigue. The level of oxygen in the blood decreases, and the skin may take on a bluish tinge (called cyanosis) and the ends of the fingers may become thick or club-shape. In most people, symptoms worsen over a period ranging from about 6 months to several years. OMIM mapping confirmed by DO. [SN]. |
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ID |
http://purl.obolibrary.org/obo/DOID_0050156 |
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comment |
OMIM mapping confirmed by DO. [SN]. |
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definition |
An idiopathic interstitial pneumonia which is a distinctive type of chronic fibrosing interstitial pneumonia with thick scarring in the lung creating a honeycomb appearance. The main symptoms start insidiously as shortness of breath on exertion, cough, and diminished stamina. Other common complaints include weight loss and fatigue. The level of oxygen in the blood decreases, and the skin may take on a bluish tinge (called cyanosis) and the ends of the fingers may become thick or club-shape. In most people, symptoms worsen over a period ranging from about 6 months to several years. |
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hasDbXref |
SNOMEDCT_US_2016_03_01:196125002 MESH:D054990 SNOMEDCT_US_2016_03_01:233721005 SNOMEDCT_US_2016_03_01:28168000 EFO:0000768 NCI:C35716 ICD9CM:516.31 UMLS_CUI:C1800706 SNOMEDCT_US_2016_03_01:426437004 OMIM:178500 NCI:C35715 SNOMEDCT_US_2016_03_01:237121003 ICD10CM:J84.112 |
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hasExactSynonym |
FIBROCYSTIC PULMONARY DYSPLASIA IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL cryptogenic fibrosing alveolitis |
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hasOBONamespace |
disease_ontology |
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id |
DOID:0050156 |
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imported from | ||
inSubset | ||
label |
idiopathic pulmonary fibrosis |
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prefixIRI |
DOID:0050156 |
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prefLabel |
idiopathic pulmonary fibrosis |
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subClassOf |