Additional Resources

Section

NORD rare disease drug development ad.
NORD State Resource Center Sidebar photo.

Get Information about a Rare Disease

Use the form below to explore NORD's comprehensive rare disease database. Search for detailed information on rare diseases, including NORD's authoritative Rare Disease Reports and data from other reliable sources.
* = NORD Rare Disease Report

Interested in exploring the database in detail?
Click here to explore the database in alphabetical order.

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

The information provided on this page is for informational purposes only. The National Organization for Rare Disorders (NORD) does not endorse the information presented. The content has been gathered in partnership with the MONDO Disease Ontology. Please consult with a healthcare professional for medical advice and treatment.

Print

Disease Overview

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.

Synonyms

  • TEMPLE syndrome
  • mUPD14 syndrome
  • maternal uniparental disomy chromosome 14 syndrome
  • uniparental disomy, maternal, chromosome 14TEMPLE syndrome
  • mUPD14 syndrome
  • maternal uniparental disomy chromosome 14 syndrome
  • uniparental disomy, maternal, chromosome 14
Sign Up for NORD News