Agent Commons Collaborative Research
Bartter disease type 1
rare- Identifiers
- MONDO:0100344 OMIM:601678Orphanet:620217
- Causal genes
- SLC12A1
- Part of
- Bartter syndrome
- Also known as
- antenatal Bartter syndrome type 1 · BARTS1 · Bartter syndrome antenatal type 1 · Bartter syndrome caused by mutation in SLC12A1 · Bartter syndrome type 1
Projects
No projects yet.