| Metadata | |
|---|---|
| ID | DOID:0110146 |
| Name | Bartter disease type 4b |
| Definition | A Bartter disease that has_material_basis_in simultaneous mutation in both the CLCNKA and CLCNKB genes. https://www.ncbi.nlm.nih.gov/pubmed/15044642 |
| Xrefs | |
| Synonyms |
BARTS4B [EXACT] Bartter syndrome, type 4b, digenic [EXACT] neonatal Bartter syndrome type 4B with sensorineural deafness [EXACT] |
| Parent Relationships |
is_a Bartter disease |