Uniparental disomies of paternal origin (Q46779): 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 do pai, e nenhum da mãe. A confirmação é observada de pares cromossômicos idênticos e combinando a um cromossomo paterno, por testes genéticos. | |||
| description / en | description / en | ||
Any disease caused by the inheritance of two homologous copies of a chromosome from the father, and none from the mother. Confirmation is by observation of identical chromosome pairs, and matching to a paternal chromosome, 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 the father, and none from the mother. Confirmation is by observation of identical chromosome pairs, and matching to a paternal chromosome, by genetic testing.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD45.1 |
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| English | Uniparental disomies of paternal origin |
Any disease caused by the inheritance of two homologous copies of a chromosome from the father, and none from the mother. Confirmation is by observation of identical chromosome pairs, and matching to a paternal chromosome, by genetic testing. |
