Overview
Bartter syndrome type 4a 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.
Extreme thirst
Always present (100%)HP:0001959
Increased urine output
Always present (100%)HP:0000103
Low blood potassium levels
Always present (100%)HP:0002900
Sensorineural deafness
Always present (100%)HP:0000407
Urine concentrating defect
Always present (100%)HP:0004727
Decreased glomerular filtration rate
HP:0012213
Foetal polyuria
HP:0001563
Generalised decreased muscle tone
HP:0001290
Global glomerulosclerosis
HP:0004737
Hydrops fetalis
HP:0001789
Hyperaldosteronism
HP:0000859
Hyperchloriduria
HP:0002914
Hypernatriuria
HP:0012605
Hypochloremia
HP:0003113
Hypokalemic hypochloremic metabolic alkalosis
HP:0004909
Hyponatremia
HP:0002902
Hyporeflexia
HP:0001265
Increased amniotic fluid index
HP:0001561
Increased urinary potassium
HP:0003081
Mental deficiency
HP:0001249
Muscular hypotonia
HP:0001252
No development of motor milestones
HP:0001270
Premature birth
HP:0001622
Reduced renal corticomedullary differentiation
HP:0005565
Renal failure
HP:0000083
Salt wasting
HP:0000127
Soft tissue swelling
HP:0000969
Tubulointerstitial scarring
HP:0005576
Undergrowth
HP:0001508
Related Conditions
Quick Facts
- SNOMED CT
- 717791000
- UMLS CUI
- C1865270
- Fully Specified Name
- Bartter syndrome type 4a (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 29
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.