Any pseudohypoaldosteronism type 2 in which the cause of the disease is a mutation in the KLHL3 gene. The disease is Monarch Disease Ontology id MONDO_0013781 (pseudohypoaldosteronism type 2D). Also known as: KLHL3 pseudohypoaldosteronism type 2, PHA2D, pseudohypoaldosteronism type 2 caused by mutation in KLHL3.