Congenital Malabsorptive Diarrhea 4
Disease ID: disease_node_19333
Connections displayed (default: 10).
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| Dbxref | ICD10CM:P78.3, MIM:610370, ORDO:83620 |
|---|---|
| Subclassof | DOID_0050737, DOID_0060774 |
| Data Source | DOID |
| Synonyms | congenital malabsorptive diarrhea due to paucity of enteroendocrine cells, congenital malabsorptive diarrhoea 4, congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells, enteric anendocrinosis |
| Doid Label | congenital malabsorptive diarrhea 4 |
| Doid 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. |
| Has Symptom | SYMP_0000570 |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_19333 |
| Doid Id | DOID_0060779 |
| Disease Has Basis In | HP_0001197 |
| Label | Congenital Malabsorptive Diarrhea 4 |
- Outgoing r'ship
HAS_SYMPTOMto/from Dysentery(ID:disease_node_2637;disease_node_2638) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Congenital Diarrhea(ID:disease_node_19331) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)