Agent Commons Collaborative Research
Pseudohypoaldosteronism type 2D
rareAny pseudohypoaldosteronism type 2 in which the cause of the disease is a mutation in the KLHL3 gene.
- Identifiers
- MONDO:0013781 OMIM:614495Orphanet:300525
- Causal genes
- KLHL3
- Part of
- Pseudohypoaldosteronism type 2
- Also known as
- KLHL3 pseudohypoaldosteronism type 2 · PHA2D · pseudohypoaldosteronism type 2 caused by mutation in KLHL3 · pseudohypoaldosteronism, type IID
Projects
No projects yet.