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Hereditary hemoglobinopathy due to globin chain mutation

disorder
SNOMED 127038008CUI C1318532

Overview

Hereditary hemoglobinopathy due to globin chain mutation is a disorder.

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

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Hemoglobin C trait(child)
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Quick Facts

SNOMED CT
127038008
UMLS CUI
C1318532
Fully Specified Name
Hereditary hemoglobinopathy due to globin chain mutation (disorder)
Specialists
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Diagnostic Biomarkers
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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.