Agent Commons Collaborative Research
Bartter disease type 2
rareAny Bartter syndrome in which the cause of the disease is a mutation in the KCNJ1 gene.
- Identifiers
- MONDO:0009424 OMIM:241200Orphanet:620220
- Causal genes
- KCNJ1
- Part of
- Bartter syndrome
- Also known as
- BARTS2 · Bartter syndrome antenatal type 2 · Bartter syndrome caused by mutation in KCNJ1 · Bartter syndrome type 2 · Bartter syndrome, type 2
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