diarrhea 3, secretory sodium, congenital

Preferred Label : diarrhea 3, secretory sodium, congenital;

MeSH note : mutation in SPINT2;

MeSH synonym : sodium diarrhea, congenital; Diarrhea 3, Secretory Sodium, Congenital, Syndromic;

Details

Origin ID

C562576;

UMLS CUI

C5441927;

Automatic exact mappings (from CISMeF team)
- Diarrhea 8, secretory sodium, congenital [OMIM Phenotype]
Currated CISMeF NLP mapping
- Congenital secretory diarrhea, sodium type (disorder) [SNOMED CT concept]
- Congenital sodium diarrhea [ORDO Disease]
- Congenital sodium diarrhoea [ICD-11 More detail]
- Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies [OMIM Phenotype]
- congenital secretory diarrhea, sodium type [SNOMED Notion]
- congenital secretory sodium diarrhea 3 [DO Concept]
MeSH term(s) associated for indexing
- abnormalities, multiple [MeSH Descriptor]
- diarrhea [MeSH Descriptor]
- metabolism, inborn errors [MeSH Descriptor]
Record concept(s)
- diarrhea 3, secretory sodium, congenital [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital secretory diarrhea, sodium type (disorder) [SNOMED CT concept]
- Congenital sodium diarrhea [ORDO Disease]
- Diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies [OMIM Phenotype]
- Diarrhea 8, secretory sodium, congenital [OMIM Phenotype]
- congenital secretory diarrhea, sodium type [SNOMED Notion]
- congenital secretory sodium diarrhea 3 [DO Concept]

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