Concept information
Terme préférentiel
Idiopathic Pulmonary Fibrosis
Type
-
mesh:Descriptor
Définition
- 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.
Concept générique
Concepts spécifiques
Synonyme(s)
- Cryptogenic Fibrosing Alveolitis
- Fibrocystic Pulmonary Dysplasia
- Fibrosing Alveolitis, Cryptogenic
- Idiopathic Fibrosing Alveolitis, Chronic Form
- Pulmonary Fibrosis, Idiopathic
Qualificatif(s) autorisé(s)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemically induced (Qualifier)
- classification (Qualifier)
- complications (Qualifier)
- congenital (Qualifier)
- diagnosis (Qualifier)
- diagnostic imaging (Qualifier)
- diet therapy (Qualifier)
- drug therapy (Qualifier)
- economics (Qualifier)
- embryology (Qualifier)
- enzymology (Qualifier)
- epidemiology (Qualifier)
- ethnology (Qualifier)
- etiology (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- metabolism (Qualifier)
- microbiology (Qualifier)
- mortality (Qualifier)
- nursing (Qualifier)
- parasitology (Qualifier)
- pathology (Qualifier)
- physiopathology (Qualifier)
- prevention & control (Qualifier)
- psychology (Qualifier)
- radiotherapy (Qualifier)
- rehabilitation (Qualifier)
- surgery (Qualifier)
- therapy (Qualifier)
- urine (Qualifier)
- veterinary (Qualifier)
- virology (Qualifier)
Traductions
-
français
-
Alvéolite fibrosante cryptogénique
-
Fibrose interstitielle diffuse idiopathique
-
FPI (Fibrose Pulmonaire Idiopathique)
-
Pneumonie interstitielle usuelle
URI
http://data.loterre.fr/ark:/67375/JVR-PRFK0DWR-M
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