Genopathy
Gene-Disorder Association · Article
Gene
MED12
Mediator Complex Subunit 12
Disorder
Non-Syndromic X-Linked Intellectual Disability
First reported 1977
Key publication · disorder Familial X-linked mental retardation with an X chromosome abnormality.Journal of medical genetics · 1977
Manually curated
Association Review

In brief

The association between MED12 (Mediator Complex Subunit 12) and Non-Syndromic X-Linked Intellectual Disability is a manually-curated gene–disease association, supported by 2 contributing sources, 1 of them expert-curated.

Sources 2
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

2 sources

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

Request access
03
MED12

The gene

1 source summary

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

Request access
04
Non-Syndromic X-Linked Intellectual Disability

The disorder

9 database identifiers

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

Request access
05
Provenance

References & sources

4 references

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

Request access