Genopathy
Gene-Disorder Association · Article
Gene
GRIN2B
Glutamate Ionotropic Receptor NMDA Type Subunit 2B
Disorder
Dystonia
Manually curatedApproved treatment annotated
Association Review

In brief

The association between GRIN2B (Glutamate Ionotropic Receptor NMDA Type Subunit 2B) and Dystonia is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 19
Compounds 1
Trials 1of 85 via GRIN2B 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
GRIN2B

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
Interventions

Therapeutics

1 compound or drug

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

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06
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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07
Provenance

References & sources

6 references

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

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