Uniparental disomies of paternal origin (Q46779)
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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 |
||
| 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. |
Statements
CID11:LD45.1
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dki-india-LD45.1
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Concluído
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13 August 2026
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