Genopathy
Gene-Disorder Association · Article
Gene
MEG3
Maternally Expressed 3
Disorder
Motor Developmental Delay Due To 14q32.2 Paternally Expressed Gene Defect
First reported 1997
Key publication · disorder Another case of maternal uniparental disomy chromosome 14 syndrome.American journal of medical genetics · 1997
Manually curated
Association Review

In brief

The association between MEG3 (Maternally Expressed 3) and Motor Developmental Delay Due To 14q32.2 Paternally Expressed Gene Defect is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 0
Compounds 0
Trials 0
Publications 0
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

Request access
02
Provenance

Evidence and sources

1 source

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

Request access
03
MEG3

The gene

1 source summary

A gene summary alongside the source descriptions it was distilled from.

Request access
04
Motor Developmental Delay Due To 14q32.2 Paternally Expressed Gene Defect

The disorder

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

Request access
05
Provenance

References & sources

2 references

Every source and publication cited across this dossier, as one numbered reference list.

Request access