Paternal uniparental disomy of chromosome 5
MONDO:0019920Paternal uniparental disomy of chromosome 5 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(5)pat, paternal uniparental disomy of chromosome type 5
0 clinical trials for this condition and its sub-types, 0 tagged with Paternal uniparental disomy of chromosome 5 itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.