Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin

disorder

SNOMED 47516005CUI C0272035

Overview

Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin is a disorder.

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

Related Conditions

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

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

Hereditary spherocytosis due to spectrin deficiency(parent)

Quick Facts

SNOMED CT: 47516005
UMLS CUI: C0272035
Fully Specified Name: Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (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.