Familial hyperaldosteronism type 2
ORPHA: 404
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with Familial hyperaldosteronism type 2, sourced from HPO and Orphanet clinical annotations.
HypertensionGlucocortocoid-insensitive primary hyperaldosteronismAbnormal circulating renin concentrationSecretory adrenocortical adenomaTinnitusEpistaxisMuscle weaknessNauseaIntracranial hemorrhageHeadacheHypokalemiaAdrenal hyperplasiaMetabolic alkalosis
Classification & Codes
Orphanet Code
ORPHA:404Familial hyperaldosteronism type 2
| Orphanet | ORPHA:404 |
| Treatments | 0 drug(s) |
| Symptoms on record | 13 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO