Pseudohypoaldosteronism type 2D

Any pseudohypoaldosteronism type 2 in which the cause of the disease is a mutation in the KLHL3 gene.

Also known as: KLHL3 pseudohypoaldosteronism type 2, PHA2D, pseudohypoaldosteronism type 2 caused by mutation in KLHL3, familial hyperkalemic hypertension, pseudohypoaldosteronism, type 2D, pseudohypoaldosteronism, type IID

11 clinical trials for this condition and its sub-types.