Genopathy
Gene-Disorder Association · Article
Gene
MYOT
Myotilin
Disorder
Neuromuscular Disease
First reported 2009
Supporting publications 1
Key publication · gene–disorder In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy.European journal of human genetics : EJHG · 2009
Key publication · disorder Effects of cortisone in certain neuromuscular disorders.Journal of the American Medical Association · 1950
Manually curated
Association Review

In brief

The association between MYOT (Myotilin) and Neuromuscular Disease is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 15
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
MYOT

The gene

1 source summary

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

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04
Neuromuscular Disease

The disorder

8 database identifiers

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

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05
Literature

Reading

1 publication

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

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06
Provenance

References & sources

4 references

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

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