Gitelman's syndrome

disorder

SNOMED 707756004CUI C0268450

Overview

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

Signs & Symptoms

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

Low blood potassium levels

Very frequent (80-99%)HP:0002900

Gastro pain

Frequent (30-79%)HP:0002027

Hypomagnesemia

Frequent (30-79%)HP:0002917

Long Q-T syndrome

Frequent (30-79%)HP:0001657

Low-to-normal BP

Frequent (30-79%)HP:0002632

Muscle weakness

Frequent (30-79%)HP:0001324

Postnatal failure to thrive

Frequent (30-79%)HP:0001508

Abnormal glucose tolerance

Occasional (5-29%)HP:0001952

Body fails to respond to insulin

Occasional (5-29%)HP:0000855

Delayed puberty

Occasional (5-29%)HP:0000823

Enuresis

Occasional (5-29%)HP:0000805

High blood Mg levels

Occasional (5-29%)HP:0002918

Low blood calcium levels

Occasional (5-29%)HP:0002901

Metabolic alkalosis

Occasional (5-29%)HP:0200114

Muscle spasm

Occasional (5-29%)HP:0003394

Nausea and vomiting

Occasional (5-29%)HP:0002017

Nocturia

Occasional (5-29%)HP:0000017

Proteinuria

Occasional (5-29%)HP:0000093

Renal potassium wasting

Occasional (5-29%)HP:0000128

Salt craving

Occasional (5-29%)HP:0030083

Abnormal deposits of calcium in the brain

Very rare (1-4%)HP:0002514

Arthritic pain

Very rare (1-4%)HP:0002829

Blurred vision

Very rare (1-4%)HP:0000622

Breakdown of skeletal muscle

Very rare (1-4%)HP:0003201

Calcium deposits in joints

Very rare (1-4%)HP:0000934

Cancer of the pancreas

Very rare (1-4%)HP:0002894

De toni-fanconi-debre syndrome

Very rare (1-4%)HP:0001994

Decreased urinary potassium

Very rare (1-4%)HP:0012364

Diabetic ketoacidosis

Very rare (1-4%)HP:0001953

Diarrhea

Very rare (1-4%)HP:0002014

Related Conditions

Renal hypocalciuria(parent)

Connective tissue hereditary disorder(parent)

Hereditary nephropathy(parent)

Recessive hereditary disorder (autosomal)(parent)

Hypokalemic alkalosis(parent)

Hypokalemic nephropathy(parent)

Primary hypomagnesemia(parent)

Quick Facts

SNOMED CT: 707756004
UMLS CUI: C0268450
Fully Specified Name: Gitelman syndrome (disorder)
Specialists: 0
Diagnostic Biomarkers: 0
HPO Phenotypes: 30

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.