Catalog
Uniparental disomies of paternal origin
Link to WHO Definition
Uniparental disomies of paternal origin – http://id.who.int/icd/entity/2028476598
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.
Parents
Children
- Paternal uniparental disomy of chromosome 5
- Paternal uniparental disomy of chromosome 1
- Paternal uniparental disomy of chromosome 6
- Paternal uniparental disomy of chromosome 20
- Paternal uniparental disomy of chromosome 7
- Paternal uniparental disomy of chromosome 14
- Paternal uniparental disomy of chromosome 11
- Paternal uniparental disomy of chromosome 21
- Paternal uniparental disomy of chromosome 13
- Paternal uniparental disomy of chromosome X
- Paternal uniparental disomy of chromosome 15
- Paternal uniparental disomy of chromosome 4