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Hereditary spherocytosis due to deficiency of protein 4.2

disorder
SNOMED 33905008CUI C0272038

Overview

Hereditary spherocytosis due to deficiency of protein 4.2 is a disorder.

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

Related Conditions

Hereditary spherocytosis(parent)
Disorder of hematopoietic structure(parent)

Quick Facts

SNOMED CT
33905008
UMLS CUI
C0272038
Fully Specified Name
Hereditary spherocytosis due to deficiency of protein 4.2 (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.