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GTR Home > Conditions/Phenotypes > Dilated cardiomyopathy 1GG

Dilated cardiomyopathy 1GG

Summary

Any familial isolated dilated cardiomyopathy in which the cause of the disease is a mutation in the SDHA gene. [from MONDO]

Available tests

52 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (52 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: CMD1GG, FP, MC2DN1, NDAXOA, PGL5, PPGL5, SDH1, SDH2, SDHF, SDHA
    Summary: succinate dehydrogenase complex flavoprotein subunit A

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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