Genopathy
Gene-Disorder Association · Article
Gene
ROR2
Receptor Tyrosine Kinase Like Orphan Receptor 2
Disorder
Brachydactyly
First reported 2003
Supporting publications 6
Key publication · gene–disorder Interstitial deletion of chromosome 9, int del(9)(9q22.31-q31.2), including the genes causing multiple basal cell nevus syndrome and Robinow/brachydactyly 1 syndrome.European journal of pediatrics · 2003
Key publication · disorder A case of brachydactyly (type Brailsford).The British journal of radiology · 1951
Manually curated
Association Review

In brief

The association between ROR2 (Receptor Tyrosine Kinase Like Orphan Receptor 2) and Brachydactyly is reported, with clinical genetic testing available.

Sources 1
Clinical variants 2
Symptoms 0
Compounds 0
Trials 0
Publications 6
01
At a glance

Association overview

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

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02
Provenance

Evidence and sources

1 source

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

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03
ROR2

The gene

1 source summary

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

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04
Brachydactyly

The disorder

4 database identifiers

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

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05
ClinVar and variant evidence

Genetic basis

2 clinical variants

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

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06
Literature

Reading

6 publications

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

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07
Provenance

References & sources

9 references

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

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