Familial hyperreninemic hypoaldosteronism type 2

disorder

SNOMED 1186812001CUI C5568607

Overview

Familial hyperreninemic hypoaldosteronism type 2 is a disorder.

Auto-generated from clinical reference data. Not a substitute for medical advice.

Related Conditions

Hyperreninemic hypoaldosteronism(parent)

Familial aldosterone deficiency(parent)

Quick Facts

SNOMED CT: 1186812001
UMLS CUI: C5568607
Fully Specified Name: Familial hyperreninemic hypoaldosteronism type 2 (disorder)
Specialists: 0
Diagnostic Biomarkers: 0

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.