Bartter disease type 3 (Q27674849)
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A Bartter disease that has material basis in homozygous or compound heterozygous mutation in the kidney chloride channel B gene (CLCNKB) on chromosome 1p36.
- BARTS3
- Bartter syndrome type 3
- classic Bartter syndrome
- Bartter Syndrome, Classic
- BARTTER SYNDROME, TYPE 3
- Bartter Syndrome, Type 3, With Hypocalciuria
- Adult Bartter syndrome
- Bartter syndrome type III
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Bartter disease type 3 |
A Bartter disease that has material basis in homozygous or compound heterozygous mutation in the kidney chloride channel B gene (CLCNKB) on chromosome 1p36. |
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