Genopathy
Gene-Disorder Association · Article
Gene
MYH7
Myosin Heavy Chain 7
Disorder
Familial Hypertrophic Cardiomyopathy
First reported 1990
Supporting publications 163
Key publication · gene–disorder A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation.Cell · 1990
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 MYH7 (Myosin Heavy Chain 7) 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 79
Symptoms 0
Compounds 0
Trials 0
Publications 163
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
MYH7

The gene

2 source summaries

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

79 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

163 publications

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

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07
Provenance

References & sources

11 references

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

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