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1172606002: Idiopathic pleuroparenchymal fibroelastosis (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4634572018 Idiopathic pleuroparenchymal fibroelastosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4634573011 Idiopathic pleuropulmonary fibroelastosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4634574017 Idiopathic pleuroparenchymal fibroelastosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4634575016 IPPFE - idiopathic pleuroparenchymal fibroelastosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399350018 A rare idiopathic interstitial pneumonia characterized by prominent subpleural and parenchymal fibroelastosis and pleural fibrosis, predominantly involving the upper lobes. Signs and symptoms include non-productive cough, dyspnea, and recurrent respiratory infections. Pneumothorax is a frequently reported complication. Pulmonary function test reveals a restrictive pattern and reduced diffusing capacity. Computed tomography shows pleural thickening with signs of fibrosis (traction bronchiectasis, architectural distortion, and loss of volume), and reticulation. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399351019 A rare idiopathic interstitial pneumonia characterised by prominent subpleural and parenchymal fibroelastosis and pleural fibrosis, predominantly involving the upper lobes. Signs and symptoms include non-productive cough, dyspnoea, and recurrent respiratory infections. Pneumothorax is a frequently reported complication. Pulmonary function test reveals a restrictive pattern and reduced diffusing capacity. Computed tomography shows pleural thickening with signs of fibrosis (traction bronchiectasis, architectural distortion, and loss of volume), and reticulation. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4634572018 Idiopathic pleuroparenchymal fibroelastosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4634573011 Idiopathic pleuropulmonary fibroelastosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4634574017 Idiopathic pleuroparenchymal fibroelastosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4634575016 IPPFE - idiopathic pleuroparenchymal fibroelastosis en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
4634579010 A rare idiopathic interstitial pneumonia with characteristics of prominent subpleural and parenchymal fibroelastosis and pleural fibrosis, predominantly involving the upper lobes. Signs and symptoms include non-productive cough, dyspnea, and recurrent respiratory infections. Pneumothorax is a frequently reported complication. Pulmonary function test reveals a restrictive pattern and reduced diffusing capacity. Computed tomography shows pleural thickening with signs of fibrosis (traction bronchiectasis, architectural distortion and loss of volume) and reticulation. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4634580013 A rare idiopathic interstitial pneumonia with characteristics of prominent subpleural and parenchymal fibroelastosis and pleural fibrosis, predominantly involving the upper lobes. Signs and symptoms include non-productive cough, dyspnoea, and recurrent respiratory infections. Pneumothorax is a frequently reported complication. Pulmonary function test reveals a restrictive pattern and reduced diffusing capacity. Computed tomography shows pleural thickening with signs of fibrosis (traction bronchiectasis, architectural distortion and loss of volume) and reticulation. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399350018 A rare idiopathic interstitial pneumonia characterized by prominent subpleural and parenchymal fibroelastosis and pleural fibrosis, predominantly involving the upper lobes. Signs and symptoms include non-productive cough, dyspnea, and recurrent respiratory infections. Pneumothorax is a frequently reported complication. Pulmonary function test reveals a restrictive pattern and reduced diffusing capacity. Computed tomography shows pleural thickening with signs of fibrosis (traction bronchiectasis, architectural distortion, and loss of volume), and reticulation. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5399351019 A rare idiopathic interstitial pneumonia characterised by prominent subpleural and parenchymal fibroelastosis and pleural fibrosis, predominantly involving the upper lobes. Signs and symptoms include non-productive cough, dyspnoea, and recurrent respiratory infections. Pneumothorax is a frequently reported complication. Pulmonary function test reveals a restrictive pattern and reduced diffusing capacity. Computed tomography shows pleural thickening with signs of fibrosis (traction bronchiectasis, architectural distortion, and loss of volume), and reticulation. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3412731001000118 Pleuroparenchymale Fibroelastose, idiopathische de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6287951000241110 fibroélastose pleuroparenchymateuse idiopathique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
6287951000241110 fibroélastose pleuroparenchymateuse idiopathique fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3412731001000118 Pleuroparenchymale Fibroelastose, idiopathische de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Idiopathic pleuroparenchymal fibroelastosis (disorder) Is a Degenerative disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic pleuroparenchymal fibroelastosis (disorder) Is a Idiopathic interstitial pneumonitis false Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic pleuroparenchymal fibroelastosis (disorder) Is a Disorder of pleura true Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic pleuroparenchymal fibroelastosis (disorder) Finding site Pleural membrane structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Idiopathic pleuroparenchymal fibroelastosis (disorder) Associated morphology Fibrosis (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Idiopathic pleuroparenchymal fibroelastosis (disorder) Finding site Structure of interstitial tissue of lung true Inferred relationship Existential restriction modifier (core metadata concept) 2
Idiopathic pleuroparenchymal fibroelastosis (disorder) Associated morphology Inflammation and consolidation (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Idiopathic pleuroparenchymal fibroelastosis (disorder) Finding site Structure of parenchyma of lung true Inferred relationship Existential restriction modifier (core metadata concept) 3
Idiopathic pleuroparenchymal fibroelastosis (disorder) Associated morphology Fibroelastosis (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Idiopathic pleuroparenchymal fibroelastosis (disorder) Is a Lung consolidation true Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic pleuroparenchymal fibroelastosis (disorder) Is a Inflammatory disorder of lower respiratory tract true Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic pleuroparenchymal fibroelastosis (disorder) Is a Interstitial lung disease true Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic pleuroparenchymal fibroelastosis (disorder) Is a Inflammation of specific body organs true Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic pleuroparenchymal fibroelastosis (disorder) Is a Idiopathic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Idiopathic pleuroparenchymal fibroelastosis (disorder) Is a Lesion of soft tissue (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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