Congenital Secretory Sodium Diarrhea 3
Disease ID: disease_node_19341
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:P78.3, MIM:270420, ORDO:103908 |
|---|---|
| Subclassof | DOID_0080015, DOID_0050129, DOID_0050737 |
| Data Source | DOID |
| Synonyms | congenital secretory sodium diarrhea 3 syndromic, congenital secretory sodium diarrhea 3 with or without other congenital anomalies, congenital secretory sodium diarrhoea 3, congenital secretory sodium diarrhoea 3 syndromic, congenital secretory sodium diarrhoea 3 with or without other congenital anomalies |
| Doid Label | congenital secretory sodium diarrhea 3 |
| Doid Description | A secretory diarrhea that has_material_basis_in homozygous or compound heterozygous mutation in the SPINT2 gene on chromosome 19q13. |
| Has Symptom | SYMP_0000570 |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_19341 |
| Doid Id | DOID_0060781 |
| Disease Has Basis In | HP_0001197 |
| Label | Congenital Secretory Sodium Diarrhea 3 |
- Outgoing r'ship
HAS_SYMPTOMto/from Dysentery(ID:disease_node_2637;disease_node_2638) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Secretory Diarrhea(ID:disease_node_19340) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Physical Disorder(ID:disease_node_13159) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease)