Overview
Familial aldosterone deficiency 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.
Increased plasma renin
Always present (100%)HP:0000848
Salt wasting
Always present (100%)HP:0000127
Hyperkalemia
Very frequent (80-99%)HP:0002153
Hypoadrenalism
Very frequent (80-99%)HP:0000846
Hyponatremia
Very frequent (80-99%)HP:0002902
Hypotension
Very frequent (80-99%)HP:0002615
Hypovolemia
Very frequent (80-99%)HP:0011106
Mineralocorticoid insufficiency
Very frequent (80-99%)HP:0004319
Poor weight gain
Very frequent (80-99%)HP:0001508
Decrease in blood pressure upon standing up
Frequent (30-79%)HP:0001278
Decreased urinary potassium
Frequent (30-79%)HP:0012364
Diarrhea
Frequent (30-79%)HP:0002014
Dullness
Frequent (30-79%)HP:0001254
Feeding difficulties
Frequent (30-79%)HP:0011968
Intermittent fever
Frequent (30-79%)HP:0001954
Metabolic acidosis
Frequent (30-79%)HP:0001942
Nausea and vomiting
Frequent (30-79%)HP:0002017
Poor growth
Frequent (30-79%)HP:0001510
Proximal tubular acidosis
Frequent (30-79%)HP:0002049
Quick Facts
- SNOMED CT
- 715343000
- UMLS CUI
- C4275180
- Fully Specified Name
- Familial aldosterone deficiency (disorder)
- Specialists
- 0
- Diagnostic Biomarkers
- 0
- HPO Phenotypes
- 19
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.