Motor developmental delay due to 14q32.2 paternally expressed gene defect

A cause of obesity that results from inheritance of two copies of chromosome 14 from the mother, and no copy of chromosome 14 from the father.

Also known as: mUPD14 syndrome, maternal uniparental disomy chromosome 14 syndrome, TEMPLE syndrome, uniparental disomy, maternal, chromosome 14

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