Pseudoprimary hyperaldosteronism

disorder

SNOMED 707747007CUI C0221043

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Research Evidence

Peer-reviewed studies linked via MeSH term "Liddle Syndrome" from the MEDLINE/PubMed database.

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Liddle syndrome with a SCNN1B mutation: a case report and systematic review.

[object Object], [object Object], [object Object] et al. · BMC Nephrol · 2025

PMID: 40696293Meta-AnalysisFull text (PMC)

Reverse Phenotypes of Patients with Genetically Confirmed Liddle Syndrome.

[object Object], [object Object], [object Object] et al. · Clin J Am Soc Nephrol · 2024

PMID: 38265765Meta-AnalysisFull text (PMC)

Identification of glycyrrhizin metabolites in humans and of a potential biomarker of liquorice-induced pseudoaldosteronism: a multi-centre cross-sectional study.

[object Object], [object Object], [object Object] et al. · Arch Toxicol · 2019

PMID: 31605160Meta-Analysis

The Epithelial Sodium Channel-An Underestimated Drug Target.

[object Object], [object Object] · Int J Mol Sci · 2023

PMID: 37175488ReviewFull text (PMC)

Defects in ubiquitination and NETosis and their associations with human diseases.

[object Object] · Pathology · 2021

PMID: 33518384Review

Exploration for the real causative agents of licorice-induced pseudoaldosteronism.

[object Object] · J Nat Med · 2021

PMID: 33481180ReviewFull text (PMC)

Monogenic Forms of Hypertension.

[object Object], [object Object] · Endocrinol Metab Clin North Am · 2019

PMID: 31655777Review

Low-Renin Hypertension.

[object Object], [object Object], [object Object] · Endocrinol Metab Clin North Am · 2019

PMID: 31655771Review

Resistant Hypertension: A Clinical Perspective.

[object Object], [object Object], [object Object] et al. · Endocrinol Metab Clin North Am · 2019

PMID: 31655778Review

[Scientific Evaluation of Crude Drugs and Kampo Medicines Using the Eastern Blotting Method and Its Application to Biological Metabolic Studies].

[object Object] · Yakugaku Zasshi · 2018

PMID: 29863039Review

Search all PubMed articles for Pseudoprimary hyperaldosteronism

Research data from MEDLINE/PubMed

Signs & Symptoms

Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.

Decreased circulating renin level

Always present (100%)HP:0003351

Hypokalemic alkalosis

Always present (100%)HP:0001949

Mineralocorticoid insufficiency

Always present (100%)HP:0004319

Abnormal heart rate

Very frequent (80-99%)HP:0011675

Dyschezia

Very frequent (80-99%)HP:0002019

High blood pressure

Very frequent (80-99%)HP:0000822

Low blood potassium levels

Very frequent (80-99%)HP:0002900

Cerebrovascular ischemia

Frequent (30-79%)HP:0002637

Kidney damage

Frequent (30-79%)HP:0000112

Muscle weakness

Frequent (30-79%)HP:0001324

Renal failure

Frequent (30-79%)HP:0000083

Tiredness

Frequent (30-79%)HP:0012378

Related Conditions

Aldosteronism(parent)

Autosomal dominant hereditary disorder(parent)

Hereditary disorder of endocrine system(parent)

Quick Facts

SNOMED CT: 707747007
UMLS CUI: C0221043
Fully Specified Name: Pseudoprimary hyperaldosteronism (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 12

Medical Disclaimer

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. Always consult with a qualified healthcare provider regarding any medical condition or treatment plan.

Clinical content is derived from the SNOMED CT clinical ontology and curated medical knowledge graphs.