Inherited pseudohypoaldosteronism
MONDO:0100323A form of pseudohypoaldosteronism that is characterized Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology.
Also known as: hereditary pseudohypoaldosteronism
5 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trialsSub-types
Pseudohypoaldosteronism type 2
(2)
Autosomal dominant pseudohypoaldosteronism type 1
(1)
Pseudohypoaldosteronism type 1
(1)
Pseudohypoaldosteronism type 2A
(0)
Pseudohypoaldosteronism type 2B
(0)
Pseudohypoaldosteronism type 2C
(0)
Pseudohypoaldosteronism type 2D
(0)
Pseudohypoaldosteronism type 2E
(0)
Pseudohypoaldosteronism, type IB1, autosomal recessive
(0)
Pseudohypoaldosteronism, type IB2, autosomal recessive
(0)
Pseudohypoaldosteronism, type IB3, autosomal recessive
(0)