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Hereditary spherocytosis due to deficiency of protein 4.2
disorderSNOMED 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.
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.