Gallbladder, agenesis of

Preferred Label : Gallbladder, agenesis of;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal dominant;

Prefixed ID : 137040;

Details

Origin ID

137040;

UMLS CUI

C0266251;

Automatic exact mappings (from CISMeF team)
- Agenesis, aplasia and hypoplasia of gallbladder [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- Absent gallbladder [HPO term]
- Agenesis of gallbladder [ICD-11 More detail]
- Agenesis of gallbladder (disorder) [SNOMED CT concept]
- Congenital absence of gallbladder (disorder) [SNOMED CT concept]
- Gallbladder agenesis [MedDRA Preferred Term]
- Isolated agenesis of gallbladder [ORDO Disease]
- congenital absence of gallbladder [SNOMED Notion]
- gallbladder, agenesis of [MeSH concept]
- gallbladder, agenesis of [MeSH Supplementary Concept]
HPO term(s)
- Abnormal abdomen morphology [HPO term]
- Autosomal dominant inheritance [HPO term]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Absent gallbladder [HPO term]
- Agenesis of gallbladder (disorder) [SNOMED CT concept]
- Congenital absence of gallbladder (disorder) [SNOMED CT concept]
- Gallbladder agenesis [MedDRA Preferred Term]
- Isolated agenesis of gallbladder [ORDO Disease]
- congenital absence of gallbladder [SNOMED Notion]
- gallbladder, agenesis of [MeSH Supplementary Concept]
- gallbladder, agenesis of [MeSH concept]

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