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

MONDO:0014541

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, 0 tagged with Motor developmental delay due to 14q32.2 paternally expressed gene defect itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Syndromic disease (7133)

Sub-types of Motor developmental delay due to 14q32.2 paternally expressed gene defect

Maternal uniparental disomy of chromosome 14 0 trials
Paternal 14q32.2 hypomethylation syndrome 0 trials
Paternal 14q32.2 microdeletion syndrome 0 trials

Including sub-types (0) Tagged with Motor developmental delay due to 14q32.2 paternally expressed gene defect (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.