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Pseudohypoaldosteronism type 2C
rareAny pseudohypoaldosteronism type 2 in which the cause of the disease is a mutation in the WNK1 gene.
- Identifiers
- MONDO:0013778 OMIM:614492Orphanet:88940
- Causal genes
- WNK1
- Part of
- Pseudohypoaldosteronism type 2
- Also known as
- PHA2C · pseudohypoaldosteronism type 2 caused by mutation in WNK1 · pseudohypoaldosteronism, type IIC · WNK1 pseudohypoaldosteronism type 2
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