Bartter syndrome type 4

disorder

SNOMED 700112007CUI C3838860

Overview

Bartter syndrome type 4 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.

Bilateral nerve deafness

Very frequent (80-99%)HP:0008619

Hyperaldosteronism

Very frequent (80-99%)HP:0000859

Hypokalemic metabolic alkalosis

Very frequent (80-99%)HP:0001960

Increased plasma renin

Very frequent (80-99%)HP:0000848

Increased plasma renin activity

Very frequent (80-99%)HP:0000841

Low blood potassium levels

Very frequent (80-99%)HP:0002900

Salt wasting

Very frequent (80-99%)HP:0000127

Urine concentrating defect

Very frequent (80-99%)HP:0004727

Birth weight less than 10th percentile

Frequent (30-79%)HP:0001518

CKD

Frequent (30-79%)HP:0012622

Delayed ability to stand

Frequent (30-79%)HP:0025335

Delayed ability to walk

Frequent (30-79%)HP:0031936

High urine prostaglandin levels

Frequent (30-79%)HP:0003527

Hydramnios

Frequent (30-79%)HP:0001561

Hypercalciuria

Frequent (30-79%)HP:0002150

Hypochloremia

Frequent (30-79%)HP:0003113

Hypomagnesemia

Frequent (30-79%)HP:0002917

Hyponatremia

Frequent (30-79%)HP:0002902

Increased urinary potassium

Frequent (30-79%)HP:0003081

Muscle weakness

Frequent (30-79%)HP:0001324

No development of motor milestones

Frequent (30-79%)HP:0001270

Peripheral hypotonia

Frequent (30-79%)HP:0001252

Poor weight gain

Frequent (30-79%)HP:0001508

Premature birth

Frequent (30-79%)HP:0001622

Acute kidney failure

Occasional (5-29%)HP:0001919

Clumsiness

Occasional (5-29%)HP:0002312

Dehydration

Occasional (5-29%)HP:0001944

Emotional lability

Occasional (5-29%)HP:0000712

End-stage renal disease

Occasional (5-29%)HP:0003774

Nasogastric tube feeding

Occasional (5-29%)HP:0040288

Related Conditions

Bartter syndrome type 4a(child)

Bartter's syndrome(parent)

Congenital sensorineural hearing loss(parent)

Hereditary hearing loss(parent)

Quick Facts

SNOMED CT: 700112007
UMLS CUI: C3838860
Fully Specified Name: Bartter syndrome type 4 (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.