Sickle cell trait (Q39533): Difference between revisions
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| description / pt-br | description / pt-br | ||
Doença causada pela herança genética de um alelo anormal do gene da hemoglobina. Esta doença não manifesta os sintomas graves da doença falciforme que ocorre nos indivíduos homozigotos. A confirmação é pela identificação da mutação através do teste genético. | |||
| description / en | description / en | ||
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. | |||
Revision as of 04:59, 13 August 2026
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.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 3A51.0 |
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| English | Sickle cell trait |
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. |
