Atrial Septal Defect 4; Asd4

Clinical Features

Top most frequent phenotypes and symptoms related to Atrial Septal Defect 4; Asd4

  • Hypertension
  • Ventricular septal defect
  • Cardiomyopathy
  • Atrial septal defect
  • Congestive heart failure
  • Abnormal heart morphology
  • Dilated cardiomyopathy
  • Mitral valve prolapse
  • Coarctation of aorta
  • Pulmonary arterial hypertension

And another 3 symptoms. If you need more information about this disease we can help you.

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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.


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Atrial Septal Defect 4; Asd4 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
CardioNext with TTN.

By Ambry Genetics (United States).

RYR2, SCN1B, SCN2B, SCN4B, SCN5A, SNTA1, TAZ, TBX1, TBX20, TBX5, TCAP, TGFB3, TMPO, TNNC1, TNNI3, TNNT2, TPM1, TRDN, TTN, TTR , (...)

View the complete list with 65 more genes
Specificity
2 %
Genes
100 %
CMNext with TTN.

By Ambry Genetics (United States).

RYR2, SCN5A, TAZ, TBX20, TCAP, TGFB3, TMPO, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL, MYOZ2, JPH2, ACTC1, LDB3, ANKRD1, ACTN2 , (...)

View the complete list with 35 more genes
Specificity
2 %
Genes
100 %
CustomNext: Cardio.

By Ambry Genetics (United States).

RYR2, SCN1B, SCN2B, SCN4B, SCN5A, SKI, SNTA1, TAZ, TBX1, TBX20, TBX5, TCAP, TGFB2, TGFB3, TGFBR1, TGFBR2, TMPO, TNNC1, TNNI3, TNNT2 , (...)

View the complete list with 86 more genes
Specificity
1 %
Genes
100 %
DCMNext with TTN.

By Ambry Genetics (United States).

SCN5A, TAZ, TBX20, TCAP, TMPO, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL, ACTC1, LDB3, ANKRD1, ACTN2, TXNRD2, MYPN, CSRP3, NKX2-5 , (...)

View the complete list with 16 more genes
Specificity
3 %
Genes
100 %
Congenital heart disease Deletion / Duplication panel.

By Connective Tissue Gene Tests (United States).

TBX1, TBX20, TBX5, TAB2, CHD7, NKX2-5, NKX2-6, ELN, GATA4, GATA6, GDF1, JAG1, NOTCH1, NOTCH2, NR2F2
Specificity
7 %
Genes
100 %
Congenital heart disease Comprehensive panel.

By Connective Tissue Gene Tests (United States).

TBX1, TBX20, TBX5, TAB2, CHD7, NKX2-5, NKX2-6, ELN, GATA4, GATA6, GDF1, JAG1, NOTCH1, NOTCH2, NR2F2
Specificity
7 %
Genes
100 %
Congenital heart disease NGS panel.

By Connective Tissue Gene Tests (United States).

TBX1, TBX20, TBX5, TAB2, CHD7, NKX2-5, NKX2-6, ELN, GATA4, GATA6, GDF1, JAG1, NOTCH1, NOTCH2, NR2F2
Specificity
7 %
Genes
100 %
Heart Diseases - panels.

By MGZ Medical Genetics Center (Germany).

RIT1, RRAS, RYR2, SCN4B, SCN5A, SCO2, SDHA, BMPR2, SGCA, SGCB, SGCD, SGCG, SLC22A5, BRAF, SLC25A3, SNTA1, SOS1, SOS2, TAZ, TBX1 , (...)

View the complete list with 137 more genes
Specificity
1 %
Genes
100 %

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Sources and references

You can check the following sources for additional information.

OMIM MESH Genetic Syndrome Finder

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