Tracheobronchomegaly

Preferred Label : Tracheobronchomegaly;

NCIt synonyms : Mounier-Kuhn Syndrome;

NCIt definition : A rare syndrome of unknown etiology, characterized by marked dilatation of the lumen of the trachea and the main bronchi. It results in bronchiectasis and recurrent lung infections.;

Details

Origin ID

C85196;

UMLS CUI

C0040587;

Automatic exact mappings (from CISMeF team)
- Congenital tracheobronchomegaly [ICD-11 More detail]
- Mounier-Kuhn syndrome [PASCAL descriptor]
- Mounier-Kuhn syndrome [MedDRA LLT]
- Tracheobronchmegaly [HPO term]
- Tracheobronchomegalia [PASCAL descriptor]
- Tracheobronchomegaly [ICD-11 Subcategory]
Currated CISMeF NLP mapping
- Congenital tracheobronchomegaly (disorder) [SNOMED CT concept]
- Mounier-Kühn syndrome [ORDO Disease]
- Tracheobronchomegaly [MedDRA Preferred Term]
- Tracheobronchomegaly [OMIM Phenotype]
- congenital tracheobronchomegaly [SNOMED Notion]
- tracheobronchomegaly [MeSH Descriptor]
- tracheobronchomegaly [MeSH concept]
Has associated anatomic sites
- Respiratory System [NCIt concept]
- Thoracic Cavity [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Mounier-Kuhn syndrome [MedDRA LLT]
- Tracheobronchomegaly [OMIM Phenotype]
- Tracheobronchomegaly [MedDRA Preferred Term]
- tracheobronchomegaly [MeSH Descriptor]
- tracheobronchomegaly [MeSH concept]
disease_has_finding
- Rare Lesion [NCIt concept]

Keyword's position in hierarchy(ies) :

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