Bartter Disease Type 4A
Disease ID: disease_node_19153
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| Dbxref | ICD10CM:E26.8, MIM:602522 |
|---|---|
| Subclassof | DOID_445 |
| Data Source | DOID |
| Synonyms | BARTS4A, BSND, Bartter syndrome type 4a, neonatal Bartter syndrome with sensorineural deafness |
| Doid Label | Bartter disease type 4a |
| Doid Description | A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the BSND gene on chromosome 1p32. |
| Disease Node Id | disease_node_19153 |
| Doid Id | DOID_0110145 |
| Label | Bartter Disease Type 4A |
- Outgoing r'ship
SUBCLASS_OFto/from Bartter Syndrome(ID:disease_node_1490) (Disease)