" /> Sickle cell trait - CISMeF





ICD-11 code : 3A51.0;

Preferred Label : Sickle cell trait;

ICD-11 definition : 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.;

ICD-11 synonym : sickle cell haemoglobin trait; haemoglobin a-s genotype; heterozygous sickle cell trait; sickle-cell heterozygous disorder; Sickle-cell disease carrier; Hb-S - [sickle cell haemoglobin] carrier; HbAS; sickle-cell trait haemoglobin disease; Hb-S carrier; HbAS - [sickle cell haemoglobin trait]; haemoglobin sickle cell trait disorder; AS - [sickle cell trait];

ICD-11 acronym : AS;

ICD-11 inclusion : sickle-cell trait with elliptocytosis or spherocytosis; HbAS - [heterozygous haemoglobin S];

Détails


Position du mot-clé dans l'(les) arborescence(s) : arborescence

Vous pouvez consulter :

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.

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30/07/2025


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