Paternal uniparental disomy of chromosome 1

Paternal uniparental disomy of chromosome 1 is an uniparental disomy of paternal origin that most likely does not have any phenotypic expression except from cases of homozygosity for a recessive disease mutation for which only father is a carrier.

Also known as: UPD(1)pat, paternal uniparental disomy of chromosome type 1

2 clinical trials for this condition and its sub-types.