diarrhea 4, malabsorptive, congenital

Preferred Label : diarrhea 4, malabsorptive, congenital;

MeSH note : mutation in NEUROG3;

MeSH synonym : enteric anendocrinosis;

Origin ID

C563673;

UMLS CUI

C1835888;

Currated CISMeF NLP mapping
- Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (disorder) [SNOMED CT concept]
- Diarrhea 4, malabsorptive, congenital [OMIM Phenotype]
- Enteric anendocrinosis [ORDO Disease]
- congenital malabsorptive diarrhea 4 [DO Concept]
MeSH term(s) associated for indexing
- diarrhea [MeSH Descriptor]
- malabsorption syndromes [MeSH Descriptor]
Record concept(s)
- diarrhea 4, malabsorptive, congenital [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells (disorder) [SNOMED CT concept]
- Diarrhea 4, malabsorptive, congenital [OMIM Phenotype]
- Enteric anendocrinosis [ORDO Disease]
- congenital malabsorptive diarrhea 4 [DO Concept]