MeSH Browser

MeSH Heading: Idiopathic Pulmonary Fibrosis
Tree Number(s): C08.381.483.652.500
Unique ID: D054990
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D054990
Annotation: PULMONARY FIBROSIS is also available
Scope Note: 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.
Entry Term(s): Cryptogenic Fibrosing Alveolitis; Familial Idiopathic Pulmonary Fibrosis; Fibrocystic Pulmonary Dysplasia; Fibrosing Alveolitis, Cryptogenic; Idiopathic Fibrosing Alveolitis, Chronic Form; Idiopathic Pulmonary Fibrosis, Familial; Interstitial Pneumonitis, Usual; Pulmonary Fibrosis, Idiopathic; Usual Interstitial Pneumonia
Previous Indexing: Pulmonary Fibrosis (1964-2008)
Public MeSH Note: 2009
History Note: 2009
Date Established: 2009/01/01
Date of Entry: 2008/07/08
Revision Date: 2022/04/28

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

congenital (CN)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

urine (UR)

veterinary (VE)

virology (VI)

Concept UI: M0511887
Scope Note: 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.
Terms: Idiopathic Pulmonary Fibrosis Preferred Term
Term UI T703056
Date07/30/2007
LexicalTag NON
ThesaurusID; Cryptogenic Fibrosing Alveolitis
Term UI T703058
Date07/30/2007
LexicalTag NON
ThesaurusID; Pulmonary Fibrosis, Idiopathic
Term UI T812632
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Fibrosing Alveolitis, Cryptogenic
Term UI T812633
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Fibrocystic Pulmonary Dysplasia
Term UI T833800
Date12/05/2012
LexicalTag NON
ThesaurusID; Idiopathic Fibrosing Alveolitis, Chronic Form
Term UI T843517
Date05/02/2013
LexicalTag NON
ThesaurusID GHR (2014)

Idiopathic Pulmonary Fibrosis MeSH Descriptor Data 2024