Hereditary elliptocytosis due to glycophorin C deficiency

disorder

SNOMED 15121005CUI C0272045

Overview

Hereditary elliptocytosis due to glycophorin C deficiency is a disorder.

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

Related Conditions

Hereditary ovalocytosis(parent)

Quick Facts

SNOMED CT: 15121005
UMLS CUI: C0272045
Fully Specified Name: Hereditary elliptocytosis due to glycophorin C deficiency (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.