aganglionosis, colonic

Preferred Label : aganglionosis, colonic;

UMLS semantic type : T019 - Congenital Abnormality;

Origin ID

M0010380;

UMLS CUI

C0085758;

Automatic exact mappings (from CISMeF team)
- Aganglionosis of colon (disorder) [SNOMED CT concept]
- Aganglionosis of large intestine (disorder) [SNOMED CT concept]
- Hirschsprung disease [PASCAL descriptor]
- Hirschsprung disease [ICD-11 Subcategory]
- Hirschsprung disease [ORDO Disease]
- hirschsprung's disease [SNOMED Notion]
Currated CISMeF NLP mapping
- Total colonic aganglionosis (disorder) [SNOMED CT concept]
Related record
- hirschsprung disease [MeSH Descriptor]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Aganglionosis of colon (disorder) [SNOMED CT concept]
- Total Colonic Aganglionosis [NCIt concept]
- Total colonic aganglionosis [HPO term]
- Total colonic aganglionosis (disorder) [SNOMED CT concept]