Pseudohypoaldosteronism
MONDO:0018638An inherited or acquired disorder of electrolyte metabolism, characterized by the inability of the renal tubules to respond to aldosterone. It is manifested by hyperkalemic metabolic acidosis, urinary salt wasting, normal or increased aldosterone secretion and normal glomerular filtration rate.
5 clinical trials for this condition and its sub-types, 3 tagged with Pseudohypoaldosteronism itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Pseudohypoaldosteronism
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Inherited pseudohypoaldosteronism 0 trials · 4 incl. sub-types
2 sub-types
- Pseudohypoaldosteronism type 1 1 trial · 2 incl. sub-types Sub-types →
- Pseudohypoaldosteronism type 2 2 trials Sub-types →
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Transient pseudohypoaldosteronism 0 trials
Most studied deeper sub-types
Autosomal dominant pseudohypoaldosteronism type 1
(1)
Pseudohypoaldosteronism type 2A
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Pseudohypoaldosteronism type 2B
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Pseudohypoaldosteronism type 2C
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Pseudohypoaldosteronism type 2D
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Pseudohypoaldosteronism type 2E
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Pseudohypoaldosteronism, type IB1, autosomal recessive
(0)
Pseudohypoaldosteronism, type IB2, autosomal recessive
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Pseudohypoaldosteronism, type IB3, autosomal recessive
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