Genopathy
Gene-Disorder Association · Article
Gene
HMGCR
3-Hydroxy-3-Methylglutaryl-CoA Reductase
Disorder
Myopathy
First reported 1991
Supporting publications 4
Key publication · gene–disorder HMG-CoA reductase inhibitor-induced myopathy in the rat: cyclosporine A interaction and mechanism studies.The Journal of pharmacology and experimental therapeutics · 1991
Key publication · disorder Effects of vitamin E deficiency and cod liver oil on myopathy in mice.Archives of pathology · 1950
Manually curated
Association Review

In brief

The association between HMGCR (3-Hydroxy-3-Methylglutaryl-CoA Reductase) and Myopathy is reported, with clinical genetic testing available.

Sources 1
Clinical variants 0
Symptoms 13
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.

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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
HMGCR

The gene

2 source summaries

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

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04
Myopathy

The disorder

10 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

4 publications

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

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06
Provenance

References & sources

8 references

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

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