Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin

disorder

SNOMED 10564005CUI C0272037

Overview

Severe 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

Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin(parent)

Quick Facts

SNOMED CT: 10564005
UMLS CUI: C0272037
Fully Specified Name: Severe 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.