Bartter Disease Type 3
Disease ID: disease_node_19154
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| Dbxref | GARD:9659, ICD10CM:E26.8, MIM:607364 |
|---|---|
| Subclassof | DOID_445 |
| Data Source | DOID |
| Synonyms | BARTS3, Bartter syndrome type 3, classic Bartter syndrome |
| Doid Label | Bartter disease type 3 |
| Doid Description | A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the kidney chloride channel B gene (CLCNKB) on chromosome 1p36. |
| Disease Node Id | disease_node_19154 |
| Doid Id | DOID_0110144 |
| Label | Bartter Disease Type 3 |
- Outgoing r'ship
SUBCLASS_OFto/from Bartter Syndrome(ID:disease_node_1490) (Disease)