LD45.1
Uniparental disomies of paternal origin
Dissomias uniparental de origem paterna
CategoryDefinition
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.
Index Terms
Uniparental disomies of paternal originPaternal uniparental disomy of chromosome 1Paternal uniparental disomy of chromosome 4Paternal uniparental disomy of chromosome 5Paternal uniparental disomy of chromosome 6Paternal uniparental disomy of chromosome 7Paternal uniparental disomy of chromosome 11Paternal uniparental disomy of chromosome 13Paternal uniparental disomy of chromosome 14Paternal uniparental disomy of chromosome 15Paternal uniparental disomy of chromosome 20Paternal uniparental disomy of chromosome 21Paternal uniparental disomy of chromosome X