Uniparental disomies of maternal origin (Q46773): Difference between revisions
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| description / pt-br | description / pt-br | ||
Qualquer doença caracterizada pela herança de duas cópias homólogas de um cromossomo da mãe, e nenhum do pai. A confirmação é feita pela observação de pares de cromossomos idênticos e pela correspondência com um cromossomo materno por meio de testes genéticos. | |||
| description / en | description / en | ||
Any disease characterised by the inheritance of two homologous copies of a chromosome from the mother, and none from the father. Confirmation is by observation of identical chromosome pairs, and matching to a maternal chromosome, by genetic testing. | |||
Revision as of 15:34, 13 August 2026
Any disease characterised by the inheritance of two homologous copies of a chromosome from the mother, and none from the father. Confirmation is by observation of identical chromosome pairs, and matching to a maternal chromosome, by genetic testing.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | LD45.0 |
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| English | Uniparental disomies of maternal origin |
Any disease characterised by the inheritance of two homologous copies of a chromosome from the mother, and none from the father. Confirmation is by observation of identical chromosome pairs, and matching to a maternal chromosome, by genetic testing. |
