hernia - CISMeF

Preferred Label : hernia;

UMLS semantic type : T190 - Anatomical Abnormality;

Origin ID

M0010259;

UMLS CUI

C0019270;

Automatic exact mappings (from CISMeF team)
- Hereditary endotheliopathy, retinopathy, nephropathy, stroke syndrome (disorder) [Inactive SNOMED CT concept]
- Hernia [ACR pathology]
- Hernia [ACR pathology]
- Hernia [ACR pathology]
- Hernia [ACR pathology]
- Hernia [ACR pathology]
- Hernia [ACR pathology]
- Hernia [ACR pathology]
- Other hernia [MedDRA LLT]
- Pseudohernia [MedDRA Preferred Term]
Currated CISMeF NLP mapping
- Hernia [PASCAL descriptor]
- Hernia [MedDRA Preferred Term]
- Hernia [ICD-10 Block (who)]
- Hernia [HPO term]
- Hernia [NCIt concept]
- Hernia NOS [MedDRA LLT]
- Hernia of abdominal cavity (disorder) [SNOMED CT concept]
- Herniae [HRDO Sign]
- Hernias [Bloc CIM-11]
- Herniated structure (morphologic abnormality) [SNOMED CT concept]
- hernia [Disease (Nov.)]
- hernia [MedlinePlus Topic]
- hernia [Radlex concept]
- hernia, nos [SNOMED Notion]
MeSH narrower concept(s)
- enterocele [MeSH concept]
Related record
- hernia [MeSH Descriptor]
Semantic type(s)
- Anatomical Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Hernia [ICD-10 Block (who)]
- Hernia [HPO term]
- Hernia [MedDRA Preferred Term]
- Hernia [NCIt concept]
- Hernia NOS [MedDRA LLT]
- Herniated structure (morphologic abnormality) [SNOMED CT concept]
- hernia [MedlinePlus Topic]
- hernia [Radlex concept]
- hernia [Disease (Nov.)]
- hernia, nos [SNOMED Notion]