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Any pseudohypoaldosteronism type 2 in which the cause of the disease is a mutation in the CUL3 gene.
Features include: Hyperkalemia, Pseudohypoaldosteronism, Hyperchloremic metabolic acidosis, and Hypertension and 2 more.
Organ System | Phenotype Count | Example Features |
|---|---|---|
Metabolism | 2 | Hyperchloremic metabolic acidosis, Metabolic acidosis |
Heart and blood vessels | 1 | Hypertension |
Pseudohypoaldosteronism type II (PHAII) is characterized by hyperkalemia despite normal glomerular filtration rate (GFR) and frequently by hypertension. More than 180 individuals and families with PHAII have been reported. The clinical presentation of PHAII is heterogeneous. The most consistent clinical feature in both children and young adults is hyperkalemia . As with essential hypertension, blood pressure is usually normal in young persons, with hypertension developing later in life. Untreated individuals with elevated blood pressure are at risk of developing complications of hypertension including cardiac disease, renal impairment, and stroke. Other associated findings in both children and adults include hyperchloremia, metabolic acidosis, and suppressed plasma renin levels.
Source: GeneReviews — "Pseudohypoaldosteronism Type II"
CUL3 encodes cullin 3 (768 aa). Core component of multiple cullin-RING-based BCR (BTB-CUL3-RBX1) E3 ubiquitin-protein ligase complexes which mediate the ubiquitination and subsequent proteasomal degradation of target proteins. Highest expression in Testis (100.6 TPM) and Cells EBV-transformed lymphocytes (31.7 TPM).
Pseudohypoaldosteronism type 2E is caused by mutations in the CUL3 gene on chromosome 2.
CUL3 is classified as a druggable target (Clinically Actionable, Enzyme, and Serine Threonine Kinase categories) with score 0.0.
No formal diagnostic criteria for PHAII have been published.
Pseudohypoaldosteronism type II (PHAII) should be suspected in individuals with the following clinical features, supportive laboratory findings, and family history. Clinical features. Hypertension (blood pressure 140/90 mm Hg) generally manifesting in adolescence or adulthood but also reported in children. Note: The absence of frank hypertension does not preclude the diagnosis.
Supportive laboratory findings
Source: GeneReviews — "Pseudohypoaldosteronism Type II"
Other causes of hyperkalemia. Hyperkalemia resulting from the following can generally be distinguished from hyperkalemia caused by PHAII on the basis of plasma renin levels, which are increased in the following conditions and suppressed in PHAII:
Source: GeneReviews — "Pseudohypoaldosteronism Type II"
Genetic testing for CUL3 is available. Testing is considered confirmatory for diagnosis.
Biomarker and diagnostic research for pseudohypoaldosteronism type 2E has been reported in the published literature.
No approved treatments are currently available for pseudohypoaldosteronism type 2E. The disease remains an area of unmet medical need.
To establish the extent of disease and needs of an individual diagnosed with pseudohypoaldosteronism type II (PHAII), the following evaluations (if not performed as part of the diagnostic evaluation) are recommended:
Serum electrolyte analysis
Noninvasive blood pressure measurement
Consultation with a clinical geneticist and/or genetic counselor
Electrolyte and blood pressure abnormalities of PHAII are often corrected with thiazide diuretics. Metabolic abnormalities and hypertension generally improve within one week. Different thiazide diuretics exist, with different dosing regimens. In general dosing is titrated to normalization of blood pressure. It is possible that dosing will need to be increased over time or that additional anti-hypertensives will be required to adequately control blood pressure. There are no established guidelines regarding age at which treatment should begin for individuals with PHAII, but affected children who have hypertension are generally treated.
See .
Control of blood pressure is important to reduce the risk for cardiovascular and renal disease and stroke.
Appropriate surveillance includes routine electrolyte and blood pressure measurements, monitored in the same manner as for any person treated with a thiazide diuretic.
Untreated individuals with PHAII should avoid excessive...
Source: GeneReviews — "Pseudohypoaldosteronism Type II"
Untreated individuals with PHAII should avoid excessive intake of foods high in salt and potassium as these may exacerbate hypertension and hyperkalemia.
Source: GeneReviews — "Pseudohypoaldosteronism Type II"
Search ClinicalTrials.gov in the US and EU Clinical Trials Register in Europe for access to information on clinical studies for a wide range of diseases and conditions. Note: There may not be clinical trials for this disorder.
Source: GeneReviews — "Pseudohypoaldosteronism Type II"
View trials for pseudohypoaldosteronism type 2E
Appropriate surveillance includes routine electrolyte and blood pressure measurements, monitored in the same manner as for any person treated with a thiazide diuretic.
Source: GeneReviews — "Pseudohypoaldosteronism Type II"
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for pseudohypoaldosteronism type 2E.
8 publications have been identified in PubMed for pseudohypoaldosteronism type 2E. Research spans Case Report / Case Series (50%), Diagnostic / Biomarker (13%), and Review / Meta-Analysis (13%).
Wu Z (2026). [PMID: 41982973](https://pubmed.ncbi.nlm.nih.gov/41982973/). *Transl Pediatr*. [Case Report / Case Series]
Cay M (2026). [PMID: 41380172](https://pubmed.ncbi.nlm.nih.gov/41380172/). *J Pediatr Endocrinol Metab*. [Case Report / Case Series]
Geronikolou S (2026). [PMID: 41569463](https://pubmed.ncbi.nlm.nih.gov/41569463/). *Hormones (Athens)*. [Diagnostic / Biomarker]
Cruz D (2025). [PMID: 41377777](https://pubmed.ncbi.nlm.nih.gov/41377777/). *Eur J Case Rep Intern Med*. [Case Report / Case Series]
Davion JB (2024). [PMID: 39553548](https://pubmed.ncbi.nlm.nih.gov/39553548/). *Heliyon*. [Case Report / Case Series]
Tetti M (2024). [PMID: 39229746](https://pubmed.ncbi.nlm.nih.gov/39229746/). *Hypertension*. [Epidemiology / Natural History]
Maeoka Y (2024). [PMID: 39205661](https://pubmed.ncbi.nlm.nih.gov/39205661/). *Am J Physiol Renal Physiol*. [Basic Science / Preclinical]
Cornelius RJ (2024). [PMID: 39699086](https://pubmed.ncbi.nlm.nih.gov/39699086/). *Compr Physiol*. [Review / Meta-Analysis]
Data assembled from 8 of 12 sources · Last updated Sep 19, 2026, 6:53 PM UTC
Online Mendelian Inheritance in Man
European rare disease database
Genetic and Rare Diseases Info Center