Hereditary spherocytosis due to spectrin deficiency

disorder

SNOMED 25266006CUI C0272032

Overview

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 spectrin deficiency(child)

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

Severe hereditary spherocytosis due to spectrin deficiency(child)

Hereditary spherocytosis(parent)

Disorder of hematopoietic structure(parent)

Quick Facts

SNOMED CT: 25266006
UMLS CUI: C0272032
Fully Specified Name: 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.