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.

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↑ Syndromic disease (7146)

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)

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