Mild hereditary spherocytosis due to spectrin deficiency

disorder

SNOMED 32648007CUI C0272033

Overview

Mild hereditary spherocytosis due to spectrin deficiency is a disorder.

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

Related Conditions

Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin(child)

Hereditary spherocytosis due to spectrin deficiency(parent)

Quick Facts

SNOMED CT: 32648007
UMLS CUI: C0272033
Fully Specified Name: Mild hereditary spherocytosis due to spectrin 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.