Genopathy
Gene-Disorder Association · Article
Gene
MYH7
Myosin Heavy Chain 7
Disorder
Distal Myopathy
First reported 2004
Supporting publications 4
Key publication · gene–disorder Mutations in the slow skeletal muscle fiber myosin heavy chain gene (MYH7) cause laing early-onset distal myopathy (MPD1).American journal of human genetics · 2004
Key publication · disorder Late hereditary distal myopathy.Proceedings of the Royal Society of Medicine · 1950
Manually curated
Association Review

In brief

The association between MYH7 (Myosin Heavy Chain 7) and Distal Myopathy is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 0
Compounds 0
Trials 0
Publications 4
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
MYH7

The gene

2 source summaries

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

Request access
04
Distal Myopathy

The disorder

8 database identifiers

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

Request access
05
Literature

Reading

4 publications

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

Request access
06
Provenance

References & sources

8 references

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

Request access