Tracheopathia osteoplastica

Preferred Label : Tracheopathia osteoplastica;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Tracheobronchopathia osteochondroplastica;

Inheritance : Autosomal dominant;

Prefixed ID : 189961;

Details

Origin ID

189961;

UMLS CUI

C3887588;

Automatic exact mappings (from CISMeF team)
- Tracheobronchopathia osteochondroplastica [ICD-11 Subcategory]
- Tracheopathia osteoplastica [PASCAL descriptor]
Currated CISMeF NLP mapping
- Tracheobroncheopathia osteoplastica (disorder) [SNOMED CT concept]
- Tracheobronchopathia osteochondroplastica [ORDO Disease]
- Tracheobronchopathia osteoplastica [MeSH concept]
- Tracheopathia osteoplastica [MedDRA LLT]
- Tracheopathia osteoplastica (disorder) [SNOMED CT concept]
- tracheobroncheopathia osteoplastica [SNOMED Notion]
- tracheobronchopathia osteoplastica [MeSH Supplementary Concept]
- tracheopathia osteoplastica [SNOMED Notion]
HPO term(s)
- Abnormality of the skeletal system [HPO term]
- Autosomal dominant inheritance [HPO term]
- Cough [HPO term]
- Dyspnea [HPO term]
- Hemoptysis [HPO term]
- Hoarse voice [HPO term]
- Recurrent pneumonia [HPO term]
- Recurrent pneumonia [HPO term]
- Wheezing [HPO term]
ORDO concept(s)
- Tracheobronchopathia osteochondroplastica [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Tracheopathia osteoplastica [MedDRA LLT]
- Tracheopathia osteoplastica (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

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