Overview
Familial hyperaldosteronism 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.
High blood pressure
Always present (100%)HP:0000822
Abnormal plasma renin
Very frequent (80-99%)HP:0040084
Familial primary hyperaldosteronism type 2
Very frequent (80-99%)HP:0011740
Secretory adrenal adenoma
Frequent (30-79%)HP:0011746
Enlarged adrenal glands
Occasional (5-29%)HP:0008221
Headache
Occasional (5-29%)HP:0002315
Intracranial haemorrhage
Occasional (5-29%)HP:0002170
Low blood potassium levels
Occasional (5-29%)HP:0002900
Metabolic alkalosis
Occasional (5-29%)HP:0200114
Muscle weakness
Occasional (5-29%)HP:0001324
Nasal hemorrhage
Occasional (5-29%)HP:0000421
Nausea
Occasional (5-29%)HP:0002018
Ringing in ears
Occasional (5-29%)HP:0000360
Hyperaldosteronism
HP:0000859
Related Conditions
Quick Facts
- SNOMED CT
- 703233008
- UMLS CUI
- C1854107
- Fully Specified Name
- Familial hyperaldosteronism type 2 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 14
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.