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
- Sickle cell trait
- Sickle-cell disease carrier
- sickle-cell heterozygous disorder
- haemoglobin a-s genotype
- Hb-S - [sickle cell haemoglobin] carrier
- sickle cell haemoglobin trait
- AS - [sickle cell trait]
- HbAS - [sickle cell haemoglobin trait]
- sickle-cell trait haemoglobin disease
- haemoglobin sickle cell trait disorder
- heterozygous sickle cell trait
- HbAS - [heterozygous haemoglobin S]
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