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GTR Home > Conditions/Phenotypes > Mitral valve prolapse, myxomatous 2

Summary

Patients with MVP2 have nonsyndromic MVP of variable severity inherited as an autosomal dominant trait. For a general phenotypic description and discussion of genetic heterogeneity of mitral valve prolapse, see MVP1 (157700). [from OMIM]

Available tests

10 tests are in the database for this condition.

Genes See tests for all associated and related genes

  • Also known as: CDH19, CDH25, CDHR6, FIB1, MMVP2, MVP2, PCDH16, VMLDS1, DCHS1
    Summary: dachsous cadherin-related 1

Clinical features

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