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GTR Home > Conditions/Phenotypes > Cardiomyopathy, familial hypertrophic, 28

Cardiomyopathy, familial hypertrophic, 28

Summary

Familial hypertrophic cardiomyopathy-28 (CMH28) is characterized by asymmetric septal hypertrophy, atrial fibrillation and nonsustained ventricular tachycardia, and risk of sudden death. Dyspnea is the most common symptom, but more than half of affected individuals are asymptomatic. Hypertrabeculation of the left ventricle with noncompaction has been observed in some patients (Ochoa et al., 2018). For a general phenotypic description and discussion of genetic heterogeneity of familial hypertrophic cardiomyopathy, see CMH1 (192600). [from OMIM]

Available tests

3 tests are in the database for this condition.

Clinical tests (3 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CMH28, FHOS2, Formactin2, FHOD3
    Summary: formin homology 2 domain containing 3

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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