Genopathy
Gene-Disorder Association · Article
Gene
GRIN2B
Glutamate Ionotropic Receptor NMDA Type Subunit 2B
Manually curated
Association Review

In brief

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

Sources 1
Clinical variants 0
Symptoms 2
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.

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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
Generalized Epilepsy

The disorder

6 database identifiers

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

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05
Provenance

References & sources

4 references

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

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