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Pseudohypoaldosteronism type 2B
rareAny pseudohypoaldosteronism type 2 in which the cause of the disease is a mutation in the WNK4 gene.
- Identifiers
- MONDO:0013777 OMIM:614491Orphanet:88939
- Causal genes
- WNK4
- Part of
- Pseudohypoaldosteronism type 2
- Also known as
- PHA2B · pseudohypoaldosteronism type 2 caused by mutation in WNK4 · pseudohypoaldosteronism, type IIB · WNK4 pseudohypoaldosteronism type 2
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