Bartter disease type 2 (Q27674848)
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A Bartter disease that has material basis in homozygous or compound heterozygous mutation in the potassium channel ROMK gene (KCNJ1) on chromosome 11q24.
- BARTS2
- Bartter syndrome type 2
- Bartter syndrome type 2 antenatal
- hyperprostaglandin E syndrome 2
- hypokalemic alkalosis with hypercalciuria 2 antenatal
- Hypokalemic Alkalosis With Hypercalciuria, Antenatal, 2
- BARTTER SYNDROME, ANTENATAL, TYPE 2
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Bartter disease type 2 |
A Bartter disease that has material basis in homozygous or compound heterozygous mutation in the potassium channel ROMK gene (KCNJ1) on chromosome 11q24. |
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