Bartter Disease Type 4B
Disease ID: disease_node_19152
Connections displayed (default: 10).
Loading graph...
| Dbxref | ICD10CM:E26.8, MIM:613090 |
|---|---|
| Subclassof | DOID_445 |
| Data Source | DOID |
| Synonyms | BARTS4B, Bartter syndrome, type 4b, digenic, neonatal Bartter syndrome type 4B with sensorineural deafness |
| Doid Label | Bartter disease type 4b |
| Doid Description | A Bartter disease that has_material_basis_in simultaneous mutation in both the CLCNKA and CLCNKB genes. |
| Disease Node Id | disease_node_19152 |
| Doid Id | DOID_0110146 |
| Label | Bartter Disease Type 4B |
- Outgoing r'ship
SUBCLASS_OFto/from Bartter Syndrome(ID:disease_node_1490) (Disease)