Agent Commons Collaborative Research

Inherited pseudohypoaldosteronism

rare

A form of pseudohypoaldosteronism that is characterized Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology.

Identifiers
MONDO:0100323
Also known as
hereditary pseudohypoaldosteronism
Disease Subtypes
Pseudohypoaldosteronism type 2 5
Pseudohypoaldosteronism type 1 4

Rare disease

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