Overview
Bartter syndrome antenatal type 2 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.
Hyperaldosteronism
Always present (100%)HP:0000859
Hypercalciuria
Always present (100%)HP:0002150
Hypokalemic metabolic alkalosis
Always present (100%)HP:0001960
Increased plasma renin
Always present (100%)HP:0000848
Low blood potassium levels
Always present (100%)HP:0002900
Nephrocalcinosis
Very frequent (80-99%)HP:0000121
Hypomagnesemia
Occasional (5-29%)HP:0002917
Birth weight less than 10th percentile
HP:0001518
Bulging forehead
HP:0011220
Calcium deposits in joints
HP:0000934
Constipation
HP:0002019
Decreased body height
HP:0004322
Dehydration
HP:0001944
Diarrhea
HP:0002014
Elevated prostaglandin E2
HP:0003566
Extreme thirst
HP:0001959
Foetal polyuria
HP:0001563
Frontal protuberance
HP:0002007
High urine prostaglandin levels
HP:0003527
Hydramnios
HP:0001561
Hyperactive renin-angiotensin system
HP:0000841
Hyperchloriduria
HP:0002914
Hypochloremia
HP:0003113
Hyposthenuria
HP:0003158
Impaired platelet aggregation
HP:0003540
Increased size of skull
HP:0000256
Increased urinary potassium
HP:0003081
Increased urine output
HP:0000103
Intermittent involuntary muscle spasm
HP:0001281
Inverted triangular face
HP:0000325
Quick Facts
- SNOMED CT
- 700109009
- UMLS CUI
- C1855849
- Fully Specified Name
- Bartter syndrome antenatal type 2 (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.