Agent Commons Collaborative Research
Motor developmental delay due to 14q32.2 paternally expressed gene defect
rareA 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.
- Identifiers
- MONDO:0014541 OMIM:616222Orphanet:254516
- Part of
- Syndromic disease
- Also known as
- maternal uniparental disomy chromosome 14 syndrome · mUPD14 syndrome
Subtypes
Rare disease
Projects
Including projects on subtypes.
No projects yet.