Left Ventricular Noncompaction 7; Lvnc7

Clinical Features

Phenotypes and symptoms related to Left Ventricular Noncompaction 7; Lvnc7

  • Right bundle branch block
  • Left ventricular noncompaction
  • Left ventricular noncompaction cardiomyopathy
  • Left posterior fascicular block

Incidence and onset information

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.


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Left Ventricular Noncompaction 7; Lvnc7 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 %
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 %
Left Ventricular Noncompaction Cardiomyopathy (LVNC) Panel.

By CeGaT GmbH (Germany).

TAZ, TNNT2, TPM1, PRDM16, ACTC1, LDB3, MIB1, DTNA, LMNA, MYBPC3, MYH7
Specificity
10 %
Genes
100 %
Left Ventricular Non-Compactation Panel.

By Health in Code (Spain).

RYR2, TAZ, TNNC1, TNNI3, TNNT2, TPM1, TTN, PRDM16, ACTC1, CASQ2, LDB3, ANKRD1, ACTN2, HCN4, MIB1, CSRP3, NKX2-5, DMD, DSP, DNAJC19 , (...)

View the complete list with 16 more genes
Specificity
3 %
Genes
100 %
Inherited Cardiovascular Diseases and Sudden Death Panel.

By Health in Code (Spain).

MRPL3, RYR2, SCN10A, SCN1B, SCN2B, SCN4B, SCN5A, BMPR1B, BMPR2, SGCA, SGCB, SGCD, SKI, SLC22A5, BRAF, SLC25A4, SNTA1, SOS1, SURF1, TAZ , (...)

View the complete list with 191 more genes
Specificity
1 %
Genes
100 %
Cardiomyopathies Panel.

By Health in Code (Spain).

MRPL3, RYR2, SCN5A, SGCA, SGCB, SGCD, SLC22A5, BRAF, SLC25A4, SOS1, SURF1, TAZ, TBX1, TBX20, TBX5, TCAP, TGFB3, KLF10, TMPO, TNNC1 , (...)

View the complete list with 129 more genes
Specificity
1 %
Genes
100 %
Cardiovascular Diseases_General Panel.

By Health in Code (Spain).

RIT1, MRPL3, RRAS, RYR1, RYR2, SAR1B, BLK, SCN10A, SCN1B, SCN2B, SCN4B, SCN5A, SCO2, SDHA, BMPR1A, BMPR1B, BMPR2, SGCA, SGCB, SGCD , (...)

View the complete list with 351 more genes
Specificity
1 %
Genes
100 %

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Sources and references

You can check the following sources for additional information.

OMIM Rare Disease Symptoms Checker

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