omphalocele - CISMeF

Preferred Label : omphalocele;

UMLS semantic type : T019 - Congenital Abnormality; T047 - Disease or Syndrome;

Origin ID

M0010270;

UMLS CUI

C0795690;

Automatic exact mappings (from CISMeF team)
- Congenital omphalocele (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- EXOMPHALOS [WHO-ART Preferred Term]
- Exomphalos [ICD-10 Sub-category]
- Exomphalos [ICD-10 Sub-category (who)]
- Exomphalos [MedDRA Preferred Term]
- Omphalocele [PASCAL descriptor]
- Omphalocele [NCIt concept]
- Omphalocele [ICD-11 Category]
- Omphalocele [HPO term]
- Omphalocele [ORDO Disease]
- Omphalocele [MedDRA LLT]
- Omphalocele/exomphalos [HRDO Sign]
- Omphalocoele [MedDRA LLT]
- omphalocele [DO Concept]
- omphalocele [Disease (Nov.)]
Has phenotype(s) (HPO)
- Usually autosomal dominant [HPO term]
Related record
- hernia, umbilical [MeSH Descriptor]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital omphalocele (disorder) [SNOMED CT concept]
- Omphalocele [NCIt concept]
- Omphalocele [HPO term]
- Omphalocele [ICD-9 code]
- Omphalocele [ORDO Disease]
- Omphalocele [MedDRA LLT]
- Omphalocoele [MedDRA LLT]
- congenital omphalocele [SNOMED Notion]