Bartter Disease Type 2
Disease ID: disease_node_19155
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| Dbxref | ICD10CM:E26.8, MIM:241200 |
|---|---|
| Subclassof | DOID_445 |
| Data Source | DOID |
| Synonyms | BARTS2, Bartter syndrome type 2, Bartter syndrome type 2 antenatal, hyperprostaglandin E syndrome 2, hypokalemic alkalosis with hypercalciuria 2 antenatal |
| Doid Label | Bartter disease type 2 |
| Doid Description | A Bartter disease that has_material_basis_in homozygous or compound heterozygous mutation in the potassium channel ROMK gene (KCNJ1) on chromosome 11q24. |
| Disease Node Id | disease_node_19155 |
| Doid Id | DOID_0110143 |
| Label | Bartter Disease Type 2 |
- Outgoing r'ship
SUBCLASS_OFto/from Bartter Syndrome(ID:disease_node_1490) (Disease)