Maternal uniparental disomy of chromosome 6
MONDO:0019912Maternal uniparental disomy of chromosome 6 is an uniparental disomy of maternal origin characterized by intrauterine growth retardation. Homozygosity for a recessive disease mutation for which only a mother is a carrier may lead to other phenotypes.
Also known as: UPD(6)mat, maternal uniparental disomy of chromosome type 6
2 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trials