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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.

Overview

Category

Ontology ID

Internal:15540

Synonyms

mUPD14 syndrome

maternal uniparental disomy chromosome 14 syndrome

TEMPLE syndrome

uniparental disomy, maternal, chromosome 14

Mapped terms

DOID:0111713

GARD:0013431

MEDGEN:863995

NCIT:C120409

OMIM:616222

Orphanet:254516

UMLS:C4015558

Child terms