Gastritis, familial giant hypertrophic

Preferred Label : Gastritis, familial giant hypertrophic;

CISMeF synonym : maladie de Ménétrier;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Menetrier disease;

Inheritance : Autosomal recessive;

Laboratory abnormalities : Hypochlorhydria; Hypoproteinemia;

Prefixed ID : 137280;

Details

Origin ID

137280;

UMLS CUI

C2936660;

Automatic exact mappings (from CISMeF team)
- Other gastritis [ICD-10 Sub-category]
- Other gastritis [ICD-10 Sub-category (who)]
Currated CISMeF NLP mapping
- GASTRITIS HYPERTROPHIC [WHO-ART Included Term]
- Gastric mucosal hypertrophy [MedDRA Preferred Term]
- Gastritis hypertrophic [MedDRA Preferred Term]
- Giant Hypertrophic Gastritis [NCIt concept]
- Giant hypertrophic gastritis [PASCAL descriptor]
- Giant hypertrophic gastritis [HPO term]
- Hypertrophic gastritis (disorder) [SNOMED CT concept]
- Menetrier disease [Disease (Nov.)]
- Menetrier disease [ACR pathology]
- Menetrier disease [ICD-11 Subcategory]
- Menetrier's disease [TUV Concept]
- Menetrier's disease [MedDRA LLT]
- Ménétrier disease [ORDO Disease]
- gastric mucosal hypertrophy [DO Concept]
- gastritis, familial giant hypertrophic [MeSH concept]
- gastritis, hypertrophic [MeSH Descriptor]
- gastritis, hypertrophic [MeSH concept]
- hypertrophic gastritis [SNOMED Notion]
DO Cross reference
- gastric mucosal hypertrophy [DO Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Giant hypertrophic gastritis [HPO term]
- Hypoproteinemia [HPO term]
- Vascular dilatation [HPO term]
ORDO concept(s)
- Ménétrier disease [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- gastritis, familial giant hypertrophic [MeSH concept]

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