Genopathy
Gene-Disorder Association · Article
Gene
DRD2
Dopamine Receptor D2
Disorder
Dystonia
Manually curatedApproved treatment annotated
Association Review

In brief

The association between DRD2 (Dopamine Receptor D2) and Dystonia is reported, with clinical genetic testing available.

Sources 1
Clinical variants 106
Symptoms 19
Compounds 1
Trials 1of 85 via DRD2 compounds
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.

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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
DRD2

The gene

2 source summaries

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

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04
Dystonia

The disorder

12 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

106 clinical variants

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

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06
Interventions

Therapeutics

1 compound or drug

Gene-targeting drugs and associated compounds, with class, approval status, mechanism, indications and trials.

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07
Human studies

Clinical trials

85 clinical trials

Clinical trials reached through the pair’s compounds, keeping disorder-targeting trials separate from other indications.

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08
Provenance

References & sources

7 references

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

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