Monarch Disease Ontology identifier MONDO_0013782 (pseudohypoaldosteronism type 2E) is any pseudohypoaldosteronism type 2 in which the cause of the disease is a mutation in the CUL3 gene. Also known as: CUL3 pseudohypoaldosteronism type 2, Cul3 pseudohypoaldosteronism type 2, PHA2E, pseudohypoaldosteronism type 2 caused by mutation in CUL3, pseudohypoaldosteronism type 2 caused by mutation in Cul3.