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Bartter syndrome type 3

disorder
SNOMED 700111000CUI C1846343

Overview

Bartter syndrome type 3 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.

Low blood potassium levels
Always present (100%)HP:0002900
Low urine calcium levels
Frequent (30-79%)HP:0003127
Abnormal sclera morphology
HP:0000591
Abnormality of retina blood vessels
HP:0008046
Abnormality of the choroid
HP:0000610
Dehydration
HP:0001944
Hyperaldosteronism
HP:0000859
Hyperchloriduria
HP:0002914
Hypokalemic metabolic alkalosis
HP:0001960
Hypotension
HP:0002615
Impaired renal tubular reabsorption of chloride
HP:0005579
Increased calcium level in kidney
Excluded (<1%)HP:0000121
Increased plasma renin
HP:0000848
Increased plasma renin activity
HP:0000841
Increased urinary potassium
HP:0003081
Increased urine output
HP:0000103
Muscle weakness, generalised
HP:0003324
Renal potassium wasting
HP:0000128
Salt wasting
HP:0000127

Related Conditions

Quick Facts

SNOMED CT
700111000
UMLS CUI
C1846343
Fully Specified Name
Bartter syndrome type 3 (disorder)
Specialists
0
Diagnostic Biomarkers
0
HPO Phenotypes
19
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.