Hernia, double inguinal

Preferred Label : Hernia, double inguinal;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant with sex influence;

Prefixed ID : 142350;

Details

Origin ID

142350;

UMLS CUI

C0860251;

Automatic exact mappings (from CISMeF team)
- Bilateral inguinal hernia [MedDRA LLT]
- Bilateral inguinal hernia (disorder) [SNOMED CT concept]
- Bilateral inguinal hernia, without obstruction or gangrene [ICD-10 Sub-category (who)]
- bilateral inguinal hernia [SNOMED Notion]
Currated CISMeF NLP mapping
- Double inguinal hernia [MedDRA LLT]
- hernia, double inguinal [MeSH concept]
- hernia, double inguinal [MeSH Supplementary Concept]
HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Inguinal hernia [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Double inguinal hernia [MedDRA LLT]
- hernia, double inguinal [MeSH Supplementary Concept]
- hernia, double inguinal [MeSH concept]

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