Familial hyperaldosteronism

disorder

SNOMED 703231005CUI C3713420

Overview

Source: MedlinePlus.gov, National Library of Medicine. Not a substitute for medical advice.

Related Conditions

Familial hyperaldosteronism type 1(child)

Familial hyperaldosteronism type 2(child)

Familial hyperaldosteronism type 3(child)

Familial hyperaldosteronism type IV(child)

Primary hyperaldosteronism(parent)

Autosomal dominant hereditary disorder(parent)

Hereditary disorder of endocrine system(parent)

Quick Facts

SNOMED CT: 703231005
UMLS CUI: C3713420
Fully Specified Name: Familial hyperaldosteronism (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.