Mitral Valve Prolapse 2; Mvp2

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Description

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 (OMIM ).

Genes related to Mitral Valve Prolapse 2; Mvp2

DCHS1

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Clinical Features

Phenotypes and symptoms related to Mitral Valve Prolapse 2; Mvp2

Congestive heart failure
Mitral valve prolapse
Mitral regurgitation

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Alternative names

Mitral Valve Prolapse 2; Mvp2 Is also known as myxomatous mitral valve prolapse 2, mitral valve prolapse, myxomatous 2, mmvp2.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Mitral Valve Prolapse 2; Mvp2 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Periventricular nodular heterotopia (NGS panel of 8 genes). By CGC Genetics (Portugal). DCHS1, ARFGEF2, ERMARD, FAT4, FLNA, FMR1, LRP2, NEDD4L Specificity 13 % Genes 100 %
Periventricular nodular heterotopia (NGS panel of 8 genes). By CGC Genetics (Portugal). DCHS1, ARFGEF2, ERMARD, FAT4, FLNA, FMR1, LRP2, NEDD4L Specificity 13 % Genes 100 %
Van Maldergem Syndrome (Cerebro-Facio-Articular Syndrome) via DCHS1 Gene Sequencing with CNV Detection. By PreventionGenetics PreventionGenetics (United States). DCHS1 Specificity 100 % Genes 100 %
Van Maldergem syndrome 1 Deletion / Duplication Test. By Connective Tissue Gene Tests (United States). DCHS1 Specificity 100 % Genes 100 %
Van Maldergem syndrome 1 NGS Test. By Connective Tissue Gene Tests (United States). DCHS1 Specificity 100 % Genes 100 %
Mitral valve prolapse 2 Comprehensive Test. By Connective Tissue Gene Tests (United States). DCHS1 Specificity 100 % Genes 100 %
Mitral valve prolapse 2 Deletion / Duplication Test. By Connective Tissue Gene Tests (United States). DCHS1 Specificity 100 % Genes 100 %
Van Maldergem syndrome 1 Comprehensive Test. By Connective Tissue Gene Tests (United States). DCHS1 Specificity 100 % Genes 100 %

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Sources and references

You can check the following sources for additional information.

MESH OMIM Rare Disease Search Engine

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