hirschsprung's disease

Preferred Label : hirschsprung's disease;

Details

Origin ID

D4-56560;

UMLS CUI

C0019569;

Automatic exact mappings (from CISMeF team)
- Aganglionosis of Auerbach's plexus (disorder) [SNOMED CT concept]
- Aganglionosis of colon (disorder) [SNOMED CT concept]
- Aganglionosis of large intestine (disorder) [SNOMED CT concept]
- Hirschsprung disease [OMIM phenotypic series]
- Hirschsprung disease, susceptibility to, 1 [OMIM Phenotype]
- Hirschsprung's disease [DO Concept]
- Long segment Hirschsprung's disease (disorder) [SNOMED CT concept]
- Macrocolon [ICD-11 More detail]
- Short segment Hirschsprung's disease (disorder) [SNOMED CT concept]
- aganglionosis, colonic [MeSH concept]
Currated CISMeF NLP mapping
- Aganglionic megacolon [HPO term]
- Congenital aganglionic megacolon (disorder) [SNOMED CT concept]
- Congenital dilatation of colon (disorder) [SNOMED CT concept]
- Congenital megacolon [MedDRA Preferred Term]
- Hirschsprung Disease [NCIt concept]
- Hirschsprung disease [PASCAL descriptor]
- Hirschsprung disease [ICD-11 Subcategory]
- Hirschsprung disease [Artificial nutrition thesaurus concept]
- Hirschsprung disease [ORDO Disease]
- Hirschsprung's disease [ICD-10 Sub-category]
- Hirschsprung's disease [MedDRA LLT]
- Hirschsprungs disease [ICD-10 Sub-category (who)]
- MEGACOLON CONGENITAL [WHO-ART Preferred Term]
- Macrocolon (disorder) [SNOMED CT concept]
- Megacolon congenital [MedDRA LLT]
- congenital aganglionosis of colon [Radlex concept]
- hirschsprung disease [MeSH Descriptor]
- hirschsprung disease [MeSH concept]
ICD-10 exact mapping(s)
- Hirschsprungs disease [ICD-10 Sub-category (who)]
Manual NTBT mappings (CISMeF)
- Non-syndromic intestinal malformation [ORDO Disease]
- Rare disease involving intestinal motility [ORDO Disease]
Metaterm(s)
- gastroenterology [CISMeF Metaterm]
- pediatrics [CISMeF Metaterm]
Référence SNOMED
- auerbach's plexus [SNOMED Notion]
- colon, nos [SNOMED Notion]
- congenital absence, nos [SNOMED Notion]
- congenital dilatation, nos [SNOMED Notion]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Aganglionic megacolon [MedDRA LLT]
- Aganglionic megacolon [HPO term]
- Aganglionosis [PASCAL descriptor]
- Aganglionosis [MedDRA LLT]
- Congenital aganglionic megacolon (disorder) [SNOMED CT concept]
- Congenital megacolon [MedDRA Preferred Term]
- Congenital megacolon (disorder) [Inactive SNOMED CT concept]
- Hirschsprung Disease [NCIt concept]
- Hirschsprung disease [ORDO Disease]
- Hirschsprung disease [PASCAL descriptor]
- Hirschsprung disease [ICD-11 Subcategory]
- Hirschsprung's disease [ICD-10 Sub-category]
- Hirschsprung's disease [DO Concept]
- Hirschsprung's disease [MedDRA LLT]
- Hirschsprungs disease [ICD-10 Sub-category (who)]
- MEGACOLON CONGENITAL [WHO-ART Preferred Term]
- Macrocolon (disorder) [SNOMED CT concept]
- Megacolon congenital [MedDRA LLT]
- Pelvirectal achalasia [MedDRA LLT]
- hirschsprung disease [MeSH concept]
- hirschsprung disease [MeSH Descriptor]

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