Uniparental disomies (Q46785): Difference between revisions
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Changed label, description and/or aliases in pt-br, en |
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| description / pt-br | description / pt-br | ||
Qualquer doença causada pela herança de duas cópias homólogas de um cromossomo de um dos pais e nenhuma do outro. A confirmação é feita pela observação de pares de cromossomos idênticos por meio de testes genéticos. | |||
| description / en | description / en | ||
Any disease caused by the inheritance of two homologous copies of a chromosome from one parent, and none from the other parent. Confirmation is by observation of identical chromosomes pairs by genetic testing. | |||
Revision as of 15:35, 13 August 2026
Any disease caused by the inheritance of two homologous copies of a chromosome from one parent, and none from the other parent. Confirmation is by observation of identical chromosomes pairs by genetic testing.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD45 |
||
| English | Uniparental disomies |
Any disease caused by the inheritance of two homologous copies of a chromosome from one parent, and none from the other parent. Confirmation is by observation of identical chromosomes pairs by genetic testing. |
