microvillus inclusion disease

Preferred Label : microvillus inclusion disease;

MeSH synonym : microvillus atrophy, congenital; davidson disease; intractable diarrhea of infancy; congenital familial protracted diarrhea with enterocyte Brush-Border abnormalities; diarrhea 2, with microvillus atrophy;

Détails

Origin ID

C537470;

UMLS CUI

C0341306;

Automatic exact mappings (from CISMeF team)
- Intractable diarrhea of infancy [ORDO Disease]
- Microvillous inclusion disease [ICD-11 More detail]
Currated CISMeF NLP mapping
- Congenital microvillous atrophy (disorder) [SNOMED CT concept]
- Diarrhea 2, with microvillus atrophy, with or without cholestasis [OMIM Phenotype]
- Microvillous atrophy [MedDRA LLT]
- Microvillous inclusion disease [MedDRA Preferred Term]
- Microvillus inclusion disease [ORDO Disease]
- microvillus inclusion disease [DO Concept]
DO Cross reference
- microvillus inclusion disease [DO Concept]
MeSH term(s) associated for indexing
- malabsorption syndromes [MeSH Descriptor]
- microvilli [MeSH Descriptor]
- mucolipidoses [MeSH Descriptor]
Record concept(s)
- Microvillus inclusion disease [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital microvillous atrophy (disorder) [SNOMED CT concept]
- Diarrhea 2, with microvillus atrophy, with or without cholestasis [OMIM Phenotype]
- Microvillous atrophy [MedDRA LLT]
- Microvillous inclusion disease [MedDRA Preferred Term]
- Microvillus inclusion disease [ORDO Disease]
- microvillus inclusion disease [DO Concept]

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