Overview
Familial hyperaldosteronism type 1 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.
Familial primary hyperaldosteronism type 1
Always present (100%)HP:0011739
High blood pressure
Always present (100%)HP:0000822
Abnormal plasma renin
Very frequent (80-99%)HP:0040084
Enlarged adrenal glands
Very frequent (80-99%)HP:0008221
Caesarean section
Occasional (5-29%)HP:0011410
Extreme thirst
Occasional (5-29%)HP:0001959
Headache
Occasional (5-29%)HP:0002315
Intracranial haemorrhage
Occasional (5-29%)HP:0002170
Low blood potassium levels
Occasional (5-29%)HP:0002900
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
Secretory adrenal adenoma
Occasional (5-29%)HP:0011746
Abnormality of the urinary system
HP:0000079
Adrenogenital syndrome
HP:0000840
Decreased circulating renin level
HP:0003351
Hyperaldosteronism
HP:0000859
Related Conditions
Quick Facts
- SNOMED CT
- 703232003
- UMLS CUI
- C3838731
- Fully Specified Name
- Familial hyperaldosteronism type 1 (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 18
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.