Overview
By MedlinePlus, National Library of Medicine
Courtesy of the National Library of Medicine. Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.
Treatments & Interventions
Signs & Symptoms
Based on Human Phenotype Ontology (HPO) disease-phenotype annotations.
Decreased body height
Very frequent (80-99%)HP:0004322
Laboratory abnormality
Very frequent (80-99%)HP:0001939
Related Conditions
Bartter syndrome type 3(child)
Hypokalemic alkalosis with hypercalciuria antenatal type 1(child)
Bartter syndrome antenatal type 2(child)
Bartter syndrome type 4(child)
Hypokalemic alkalosis(parent)
Hypochloremic alkalosis(parent)
Recessive hereditary disorder (autosomal)(parent)
Hypercalciuria(parent)
Hereditary nephropathy(parent)
Renal tubular disorder(parent)
Metabolic renal disease(parent)
Renal impairment(parent)
Quick Facts
- SNOMED CT
- 707742001
- UMLS CUI
- C0004775
- Fully Specified Name
- Bartter syndrome (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 2
- Known Treatments
- 4
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.