Genopathy
Gene-Disorder Association · Article
Gene
MYBPC3
Myosin Binding Protein C3
Disorder
Familial Hypertrophic Cardiomyopathy
First reported 1995
Supporting publications 139
Key publication · gene–disorder Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy.Nature genetics · 1995
Key publication · disorder Surgical treatment of idiopathic hypertrophic subaortic stenosis: technic and hemodynamic results of subaortic ventriculomyotomy.Annals of surgery · 1961
Manually curated
Association Review

In brief

The association between MYBPC3 (Myosin Binding Protein C3) and Familial Hypertrophic Cardiomyopathy is well established and manually curated, drawing on a single expert-curated source, which records pathogenic variants.

Sources 1
Clinical variants 154
Symptoms 0
Compounds 0
Trials 0
Publications 139
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
MYBPC3

The gene

1 source summary

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

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04
Familial Hypertrophic Cardiomyopathy

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
ClinVar and variant evidence

Genetic basis

154 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

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06
Literature

Reading

139 publications

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

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07
Provenance

References & sources

10 references

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

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