Search
Descriptor English: Idiopathic Interstitial Pneumonias
Descriptor Spanish: Neumonías Intersticiales Idiopáticas
Descriptor neumonías intersticiales idiopáticas
Scope note: Grupo de neumopatías intersticiales de etiología desconocida. Existen varias entidades con diversos patrones de inflamación y fibrosis. Se clasifican por sus diferentes características clínicas, radiológicas, anatomopatológicas y de pronóstico. Incluyen la FIBROSIS PULMONAR IDIOPÁTICA, la NEUMONÍA CRIPTOGÉNICA ORGANIZADA y otras.
Descriptor Portuguese: Pneumonias Intersticiais Idiopáticas
Descriptor French: Pneumopathies interstitielles idiopathiques
Entry term(s): Idiopathic Interstitial Pneumonia
Interstitial Pneumonia, Idiopathic
Interstitial Pneumonias, Idiopathic
Pneumonia, Idiopathic Interstitial
Pneumonias, Idiopathic Interstitial
Tree number(s): C08.381.483.652.500.750
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D054988
Scope note: A group of interstitial lung diseases with no known etiology. There are several entities with varying patterns of inflammation and fibrosis. They are classified by their distinct clinical-radiological-pathological features and prognosis. They include IDIOPATHIC PULMONARY FIBROSIS; CRYPTOGENIC ORGANIZING PNEUMONIA; and others.
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CN congenital
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Lung Diseases, Interstitial (1993-2008)
Pulmonary Fibrosis (1972-1992)
Public MeSH Note: 2009
History Note: 2009
DeCS ID: 53082
Unique ID: D054988
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2009/01/01
Date of Entry: 2008/07/08
Idiopathic Interstitial Pneumonias - Preferred
Concept UI M0511856
Scope note A group of interstitial lung diseases with no known etiology. There are several entities with varying patterns of inflammation and fibrosis. They are classified by their distinct clinical-radiological-pathological features and prognosis. They include IDIOPATHIC PULMONARY FIBROSIS; CRYPTOGENIC ORGANIZING PNEUMONIA; and others.
Preferred term Idiopathic Interstitial Pneumonias
Entry term(s) Idiopathic Interstitial Pneumonia
Interstitial Pneumonia, Idiopathic
Interstitial Pneumonias, Idiopathic
Pneumonia, Idiopathic Interstitial
Pneumonias, Idiopathic Interstitial



We want your feedback on the new DeCS / MeSH website

We invite you to complete a survey that will take no more than 3 minutes.

Go to survey