Cardiomyopathy, Familial Hypertrophic, 19; Cmh19

Clinical Features

Phenotypes and symptoms related to Cardiomyopathy, Familial Hypertrophic, 19; Cmh19

  • Asymmetric septal hypertrophy

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.

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.

Cardiomyopathy, Familial Hypertrophic, 19; Cmh19 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Cardiomyopathy NGS Multi-Gene Panel (50 genes), Sequence & CNV analysis.

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam (Netherlands).

SCN5A, SGCD, TAZ, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL, MYOZ2, PRDM16, JPH2, ACTC1, CAV3, LDB3, ANKRD1, ACTN2, HCN4 , (...)

View the complete list with 31 more genes
Specificity
2 %
Genes
100 %
Cardiomyopathy, familial hypertrophic (sequence analysis of CALR3 gene).

By CGC Genetics (Portugal).

CALR3
Specificity
100 %
Genes
100 %
Comprehensive Cardiology Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

RYR1, RYR2, SCN1B, SCN2B, SCN4B, SCN5A, SCO2, SGCD, SGCG, BRAF, SLC25A4, SNTA1, SOS1, SREBF2, TAZ, TBX3, TBX5, TCAP, TGFB2, TGFB3 , (...)

View the complete list with 143 more genes
Specificity
1 %
Genes
100 %
Pan Cardiomyopathy Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics (United States).

RYR2, SCN5A, SCO2, SGCD, SGCG, BRAF, SOS1, TAZ, TCAP, TGFB3, TGFBR2, TMPO, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL, MYOZ2 , (...)

View the complete list with 62 more genes
Specificity
2 %
Genes
100 %
Cardiomyopathy panel.

By Genome Diagnostics Laboratory University Medical Center Utrecht (Netherlands).

RYR2, SCN5A, SGCD, TAZ, TCAP, TMPO, TNNC1, TNNI3, TNNT2, TPM1, MYOT, TTR, VCL, MYOZ2, MYOZ1, JPH2, ACTC1, CASQ2, CAV3, LDB3 , (...)

View the complete list with 41 more genes
Specificity
2 %
Genes
100 %
Cardiomyopathy, familial hypertrophic, 19.

By Centogene AG - the Rare Disease Company (Germany).

CALR3
Specificity
100 %
Genes
100 %
Cardiomyopathy, hypertrophic Panel.

By CeGaT GmbH (Germany).

TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL, MYOZ2, JPH2, ACTC1, CAV3, LDB3, ANKRD1, MYLK2, ACTN2, CALR3, MYPN, CSRP3, NEXN , (...)

View the complete list with 10 more genes
Specificity
4 %
Genes
100 %
Hypertrophic Cardiomyopathy.

By Asper Biogene Asper Biogene LLC (Estonia).

SLC25A4, SOS1, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL, MYOZ2, JPH2, ACTC1, CAV3, LDB3, ANKRD1, MYLK2, ACTN2, CALR3, AGK , (...)

View the complete list with 15 more genes
Specificity
3 %
Genes
100 %

You can get up to 17 more panels with our dedicated tool

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Search Engine

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