Pseudohypoaldosteronism type 2D

MONDO:0013781

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

1 clinical trial for this condition and its sub-types, 0 tagged with Pseudohypoaldosteronism type 2D itself.

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↑ Pseudohypoaldosteronism type 2 (2)

Including sub-types (1) Tagged with Pseudohypoaldosteronism type 2D (0)

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