Familial primary hypomagnesemia with normocalciuria

disorder

SNOMED 717788000CUI C4305528

Overview

Familial primary hypomagnesemia with normocalciuria is a disorder.

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

Related Conditions

Familial primary hypomagnesemia with normocalciuria and normocalcemia(child)

Autosomal hereditary disorder(parent)

Primary hypomagnesemia(parent)

Quick Facts

SNOMED CT: 717788000
UMLS CUI: C4305528
Fully Specified Name: Familial primary hypomagnesemia with normocalciuria (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.