Congenital Diarrhea 7 With Exudative Enteropathy
Disease ID: disease_node_19334
Connections displayed (default: 10).
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| Dbxref | ICD10CM:P78.3, MIM:615863, ORDO:329242 |
|---|---|
| Subclassof | DOID_0050737, DOID_0060774 |
| Data Source | DOID |
| Synonyms | congenital chronic diarrhea with exudative enteropathy, congenital chronic diarrhea with protein-losing enteropathy, congenital chronic diarrhoea with exudative enteropathy, congenital chronic diarrhoea with protein-losing enteropathy, congenital diarrhoea 7 with exudative enteropathy |
| Doid Label | congenital diarrhea 7 with exudative enteropathy |
| Doid Description | A congenital diarrhea characterized by watery diarrhea, protein-losing enteropathy, patchy areas of dystrophic microvilli in the duodenum and patchy areas of villous atrophy that has_material_basis_in homozygous mutation in the DGAT1 gene on chromosome 8q24.3. |
| Has Symptom | SYMP_0000570 |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_19334 |
| Doid Id | DOID_0060778 |
| Disease Has Basis In | HP_0001197 |
| Label | Congenital Diarrhea 7 With Exudative Enteropathy |
- Outgoing r'ship
HAS_SYMPTOMto/from Dysentery(ID:disease_node_2637;disease_node_2638) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Congenital Diarrhea(ID:disease_node_19331) (Disease)