Genopathy
Gene-Disorder Association · Article
Gene
FOXO1
Forkhead Box O1
Disorder
Rhabdomyosarcoma
First reported 1995
Supporting publications 10
Key publication · gene–disorder Detection of the t(2;13)(q35;q14) and PAX3-FKHR fusion in alveolar rhabdomyosarcoma by fluorescence in situ hybridization.Genes, chromosomes & cancer · 1995
Key publication · disorder Embryonal rhabdomyosarcoma of the head and neck in children and adolescents.Cancer · 1950
Manually curated
Association Review

In brief

The association between FOXO1 (Forkhead Box O1) and Rhabdomyosarcoma is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 0
Compounds 0
Trials 0
Publications 10
01
At a glance

Association overview

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

Request access
02
Provenance

Evidence and sources

1 source

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

Request access
03
FOXO1

The gene

1 source summary

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

Request access
04
Rhabdomyosarcoma

The disorder

13 database identifiers

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

Request access
05
Literature

Reading

10 publications

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

Request access
06
Provenance

References & sources

11 references

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

Request access