Overview
Familial hyperaldosteronism 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.
Abnormal plasma renin
Always present (100%)HP:0040084
Decreased circulating renin level
Always present (100%)HP:0003351
High blood pressure
Always present (100%)HP:0000822
Hyperaldosteronism
Always present (100%)HP:0000859
Glucocortocoid-insensitive primary hyperaldosteronism
Very frequent (80-99%)HP:0011740
Low blood potassium levels
Very frequent (80-99%)HP:0002900
Extreme thirst
Occasional (5-29%)HP:0001959
Frequent nosebleeds
Occasional (5-29%)HP:0000421
Headache
Occasional (5-29%)HP:0002315
Hypercalciuria
Occasional (5-29%)HP:0002150
Increased urine output
Occasional (5-29%)HP:0000103
Intracranial haemorrhage
Occasional (5-29%)HP:0002170
Left ventricular wall hypertrophy
Occasional (5-29%)HP:0001712
Long Q-T syndrome
Occasional (5-29%)HP:0001657
Metabolic acidosis
Occasional (5-29%)HP:0001942
Metabolic alkalosis
Occasional (5-29%)HP:0200114
Muscle weakness
Occasional (5-29%)HP:0001324
Nausea
Occasional (5-29%)HP:0002018
Ringing in ears
Occasional (5-29%)HP:0000360
Enlarged adrenal glands
HP:0008221
Related Conditions
Quick Facts
- SNOMED CT
- 703234002
- UMLS CUI
- C3838758
- Fully Specified Name
- Familial hyperaldosteronism type 3 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 20
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.