3A51.0 Sickle cell trait

International Classification of Diseases for Mortality and Morbidity Statistics, 11th Revision, v2024-01


A disease caused by genetic inheritance of one abnormal allele of the haemoglobin gene. This disease does not display the severe symptoms of sickle cell disease that occurs in homozygous individuals. Confirmation is by identification of mutation through genetic testing.

synonyms

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