Genopathy
Gene-Disorder Association · Article
Gene
MSH2
MutS Homolog 2
Disorder
Cervical Cancer
First reported 2000
Supporting publications 1
Key publication · gene–disorder Msh2, Mlh1, Fhit, p53, Bcl-2, and Bax expression in invasive and in situ squamous cell carcinoma of the uterine cervix.Clinical cancer research : an official journal of the American Association for Cancer Research · 2000
Key publication · disorder Pregnancy following cervix cancer; report of two cases treated in a preinvasive stage.Surgery, gynecology & obstetrics · 1950
Manually curated
Association Review

In brief

The association between MSH2 (MutS Homolog 2) and Cervical Cancer is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 3
Compounds 0
Trials 0
Publications 1
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
MSH2

The gene

1 source summary

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

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04
Cervical Cancer

The disorder

15 database identifiers

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

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05
Phenotype

Clinical features

2 clinical features

The disorder’s clinical features (HPO) grouped by body system, each with observed frequency and penetrance.

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06
Literature

Reading

1 publication

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

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07
Provenance

References & sources

5 references

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

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