Genopathy
Gene-Disorder Association · Article
Gene
FGFR2
Fibroblast Growth Factor Receptor 2
Disorder
Glioma
First reported 1950
Key publication · disorder [Contribution to the cytokaryologic study of glioma. Note II. Karyology of some tumoral cytotypes of glioma and of the hyperplastic astrocytary glia].Rivista di anatomia patologica e di oncologia · 1950
Manually curatedApproved treatment annotated
Association Review

In brief

The association between FGFR2 (Fibroblast Growth Factor Receptor 2) and Glioma is a manually-curated gene–disease association, with its 2 contributing sources — 1 of them expert-curated — recording likely-pathogenic variants.

Sources 2
Clinical variants 0
Symptoms 0
Compounds 1
Trials 12of 263 via FGFR2 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

2 sources

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

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03
FGFR2

The gene

3 source summaries

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

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04
Glioma

The disorder

1 database identifier

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

263 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

7 references

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

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