Genopathy
Gene-Disorder Association · Article
Gene
MECOM
MDS1 And EVI1 Complex Locus
Disorder
Radioulnar Synostosis With Amegakaryocytic Thrombocytopenia 2
First reported 2010
Supporting publications 4
Key publication · disorder A case of congenital bone marrow failure with radio-ulnar synostosis.International journal of hematology · 2010
Manually curated
Association Review

In brief

The association between MECOM (MDS1 And EVI1 Complex Locus) and Radioulnar Synostosis With Amegakaryocytic Thrombocytopenia 2 is well established and manually curated, with its 4 contributing sources — 3 of them expert-curated — recording a known molecular basis, pathogenic variants, and causative variation.

Sources 4
Clinical variants 33
Symptoms 28
Compounds 0
Trials 0
Publications 4
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

4 sources

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

Request access
03
MECOM

The gene

1 source summary

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

Request access
04
Radioulnar Synostosis With Amegakaryocytic Thrombocytopenia 2

The disorder

7 database identifiers

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

Request access
05
Phenotype

Clinical features

14 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

Request access
06
ClinVar and variant evidence

Genetic basis

33 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

Request access
07
Mechanism overlap

Shared mechanisms

Biological pathways and phenotype concepts shared by the gene and the disorder, with supporting publications.

Request access
08
Literature

Reading

4 publications

Publications linking the gene and the disorder, with title, authors, journal, year and citation metrics.

Request access
09
Provenance

References & sources

10 references

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

Request access