Familial hypokalemic alkalosis, Gullner type

disorder

SNOMED 81987005CUI C0268444

Overview

Familial hypokalemic alkalosis, Gullner type is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Signs & Symptoms

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

Abnormal magnesium metabolism

HP:0004921

Elevated prostaglandin E2

HP:0003566

Hypokalemic alkalosis

HP:0001949

Increased plasma renin

HP:0000848

Low blood potassium levels

HP:0002900

Muscle spasm

HP:0003394

Nausea

HP:0002018

Selective proximal tubular damage

HP:0000114

Tiredness

HP:0012378

Vomiting

HP:0002013

Related Conditions

Specific renal tubule transport defect(parent)

Recessive hereditary disorder (autosomal)(parent)

Familial disease(parent)

Hypokalemic alkalosis(parent)

Hereditary nephropathy(parent)

Metabolic renal disease(parent)

Quick Facts

SNOMED CT: 81987005
UMLS CUI: C0268444
Fully Specified Name: Familial hypokalemic alkalosis, Gullner type (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 10

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.