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GTR Home > Conditions/Phenotypes > Hypertrophic cardiomyopathy 26

Hypertrophic cardiomyopathy 26

Synonyms
Cardiomyopathy, familial hypertrophic, 26

Summary

Familial cardiomyopathy caused by mutation in the FLNC gene has been described as hypertrophic, restrictive, dilated, or arrhythmogenic right ventricular cardiomyopathy. Affected individuals, especially those with dilated cardiomyopathy, are at risk for arrhythmias and sudden death. Arrhythmias without cardiomyopathy, and left ventricular noncompaction, have also been reported (Ortiz-Genga et al., 2016; Verdonschot et al., 2020). [from OMIM]

Available tests

38 tests are in the database for this condition.

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Clinical tests (38 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: ABP-280, ABP280A, ABPA, ABPL, ARVC15, CMH26, FLN2, MFM5, MPD4, RCM5, FLNC
    Summary: filamin C

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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