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HPFH A gamma beta^+^ thalassemia

disorder
SNOMED 39586009CUI C0272000

Quick Facts

SNOMED CT
39586009
UMLS CUI
C0272000
Fully Specified Name
Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (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.