congenital malabsorptive diarrhea 4
Information
- Disease name
- congenital malabsorptive diarrhea 4
- Disease ID
- DOID:0060779
- Description
- "A congenital diarrhea characterized by chronic unremitting malabsorptive diarrhea and a profound dysgenesis of the enteroendocrine cells that has_material_basis_in mutation in the gene encoding neurogenin-3 (NEUROG3) on chromosome 10q21.3." [url:https\://www.ncbi.nlm.nih.gov/pubmed/16855267]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:0060774
- Cross Reference ID (Disease Ontology)
- ICD10CM:P78.3
- Cross Reference ID (Disease Ontology)
- MIM:610370
- Cross Reference ID (Disease Ontology)
- ORDO:83620
- Exact Synonym (Disease Ontology)
- congenital malabsorptive diarrhea due to paucity of enteroendocrine cells
- Exact Synonym (Disease Ontology)
- congenital malabsorptive diarrhoea 4
- Exact Synonym (Disease Ontology)
- congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells
- Exact Synonym (Disease Ontology)
- enteric anendocrinosis