interstitial pneumonia - CISMeF

CISMeF

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Interstitial pneumoniaSNOMED Notion

Preferred Label : interstitial pneumonia;

Details

Origin ID

D2-60680;

UMLS CUI

C0206061;

Automatic exact mappings (from CISMeF team)
- Desquamative interstitial pneumonia (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Interstitial Lung Disease [NCIt concept]
- Interstitial Pneumonia [NCIt concept]
- Interstitial lung disease [TUV Term]
- Interstitial lung disease [TUV Concept]
- Interstitial lung disease [ORDO Disease]
- Interstitial pneumonia [MedDRA LLT]
- Interstitial pneumonia (disorder) [SNOMED CT concept]
- Interstitial pneumonitis [PASCAL descriptor]
- Interstitial pneumonitis [MedDRA LLT]
- Interstitial pulmonary disease, unspecified [ICD-10 Sub-category (who)]
- PNEUMONIA INTERSTITIAL [WHO-ART Included Term]
- Pneumonia interstitial [MedDRA LLT]
- Pulmonary Fibrosis [NCIt concept]
- interstitial lung disease [Radlex concept]
- interstitial lung diseases [MedlinePlus Topic]
- interstitial pneumonia [Radlex concept]
- interstitial pneumonia [Disease (Nov.)]
- lung diseases, interstitial [MeSH Descriptor]
- lung diseases, interstitial [MeSH concept]
- pneumonia, interstitial [MeSH concept]
ICD-10 exact mapping(s)
- Other specified interstitial pulmonary diseases [ICD-10 Sub-category (who)]
Manual BTNT mappings - CISMeF
- Adult acute respiratory distress syndrome [ORDO Disease]
- Chronic pneumonitis of infancy [ORDO Disease]
- Congenital alveolar capillary dysplasia [ORDO Disease]
- Idiopathic interstitial pneumonia [ORDO Disease]
- Lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome [ORDO Disease]
- Neuroendocrine cell hyperplasia of infancy [ORDO Disease]
- Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies [ORDO Disease]
- Pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome [ORDO Disease]
- Pulmonary interstitial glycogenosis [ORDO Disease]
- Rare allergic respiratory disease [ORDO Disease]
- Secondary interstitial lung disease in childhood and adulthood associated with a connective tissue disease [ORDO Disease]
Manual NTBT mappings (CISMeF)
- Rare pulmonary disease [ORDO Disease]
Metaterm(s)
- pulmonology [CISMeF Metaterm]
Référence SNOMED
- chronic inflammation, nos [SNOMED Notion]
- fibrosis, nos [SNOMED Notion]
- interstitial tissue of lung, nos [SNOMED Notion]
SNOMED CT concept
- Interstitial pneumonia (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Interstitial Pneumonia [NCIt concept]
- Interstitial pneumonia [MedDRA LLT]
- Interstitial pneumonia (disorder) [SNOMED CT concept]
- Interstitial pneumonitis [MedDRA LLT]
- Interstitial pneumonitis [HPO term]
- PNEUMONIA INTERSTITIAL [WHO-ART Included Term]
- Pneumonia interstitial [MedDRA LLT]
- interstitial pneumonia [Disease (Nov.)]
- pneumonia, interstitial [MeSH concept]
Validated automatic mappings to NTBT
- interstitial lung disorder [Disease (Nov.)]

Keyword's position in hierarchy(ies) :

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13/05/2024

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