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Inherited pseudohypoaldosteronism

MONDO:0100323

A 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, 0 tagged with Inherited pseudohypoaldosteronism itself.

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Where it sits in the disease tree

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Part of

↑ Inherited kidney disorder (317) ↑ Pseudohypoaldosteronism (5)

Sub-types of Inherited pseudohypoaldosteronism

Pseudohypoaldosteronism type 2 2 trials
5 sub-types
- Pseudohypoaldosteronism type 2A 0 trials
- Pseudohypoaldosteronism type 2B 0 trials
- Pseudohypoaldosteronism type 2C 0 trials
- Pseudohypoaldosteronism type 2D 0 trials
- Pseudohypoaldosteronism type 2E 0 trials
Pseudohypoaldosteronism type 1 1 trial · 2 incl. sub-types
4 sub-types
- Autosomal dominant pseudohypoaldosteronism type 1 1 trial
- Pseudohypoaldosteronism, type IB1, autosomal recessive 0 trials
- Pseudohypoaldosteronism, type IB2, autosomal recessive 0 trials
- Pseudohypoaldosteronism, type IB3, autosomal recessive 0 trials

Including sub-types (5) Tagged with Inherited pseudohypoaldosteronism (0)

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