Cardiomyopathy, Dilated, 1o; Cmd1o
Clinical Features
Phenotypes and symptoms related to Cardiomyopathy, Dilated, 1o; Cmd1o
- Congestive heart failure
- Dilated cardiomyopathy
- Ventricular tachycardia
- Impaired myocardial contractility
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
Cardiomyopathy, Dilated, 1o; Cmd1o Is also known as cardiomyopathy, dilated, with ventricular tachycardia.
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, Dilated, 1o; Cmd1o Recommended genes panels
Panel Name, Specifity and genes Tested/covered |
---|
Brugada Syndrome Panel.
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).
SCN1B, SCN2B, SCN5A, CACNA1C, CACNB2, SLMAP, HCN4, TRPM4, SCN3B, GPD1L, ABCC9, KCND3, KCNE3, KCNH2, KCNJ8, PKP2
Specificity
7 %
Genes
100 % |
Comprehensive Cardiac Panel.
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center (United States).
RIT1, RYR2, SCN1B, SCN2B, SCN4B, SCN5A, SGCD, SLC22A5, BRAF, SNTA1, SOS1, TAZ, TCAP, TGFB3, TNNC1, TNNI3, TNNT2, TPM1, TRDN, TTN , (...)
View the complete list with 86 more genes
Specificity
1 %
Genes
100 % |
Dilated cardiomyopathy - full panel.
By CHEO Genetics Diagnostic Laboratory Children's Hospital of Eastern Ontario (Canada).
SGCD, TAZ, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN, VCL, ACTC1, LDB3, ACTN2, CSRP3, CTF1, RBM20, DES, NEXN, EMD, ABCC9, LAMP2 , (...)
View the complete list with 5 more genes
Specificity
4 %
Genes
100 % |
Dilated cardiomyopathy - familial variant analysis.
By CHEO Genetics Diagnostic Laboratory Children's Hospital of Eastern Ontario (Canada).
SGCD, TAZ, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN, VCL, ACTC1, LDB3, ACTN2, CSRP3, CTF1, RBM20, DES, NEXN, EMD, ABCC9, LAMP2 , (...)
View the complete list with 5 more genes
Specificity
4 %
Genes
100 % |
Pan-cardiomyopathy panel.
By CHEO Genetics Diagnostic Laboratory Children's Hospital of Eastern Ontario (Canada).
RYR2, SGCD, TAZ, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL, MYOZ2, ACTC1, CASQ2, CAV3, LDB3, ANKRD1, MYLK2, ACTN2, CRYAB , (...)
View the complete list with 25 more genes
Specificity
3 %
Genes
100 % |
Cardiomyopathy Panel.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States).
RYR2, SCN1B, SCN4B, SCN5A, SCO2, SGCD, SKI, BRAF, SNTA1, SOS1, SURF1, TAZ, TCAP, TGFB2, TGFB3, TGFBR1, TGFBR2, TMPO, TNNC1, TNNI3 , (...)
View the complete list with 92 more genes
Specificity
1 %
Genes
100 % |
Dilated Cardiomyopathy Panel.
By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States).
SCN5A, SGCD, TAZ, TCAP, TMPO, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL, ACTC1, LDB3, ANKRD1, ACTN2, NEBL, TXNRD2, PDLIM3, MYPN , (...)
View the complete list with 24 more genes
Specificity
3 %
Genes
100 % |
Dilated Cardiomyopathy Panel (30 genes).
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center (United States).
SCN5A, SGCD, TAZ, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN, VCL, ACTC1, LDB3, ANKRD1, ACTN2, NEBL, MYPN, CRYAB, CSRP3, RBM20, DES , (...)
View the complete list with 10 more genes
Specificity
4 %
Genes
100 % |
You can get up to 121 more panels with our dedicated tool
Learn moreSources and references
You can check the following sources for additional information.
MESH OMIM Rare Disease Symptoms CheckerIf you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like POLYDACTYLY, POSTAXIAL, TYPE A1; PAPA1 METABOLIC ENCEPHALOMYOPATHIC CRISES, RECURRENT, WITH RHABDOMYOLYSIS, CARDIAC ARRHYTHMIAS, AND NEURODEGENERATION; MECRCN EHLERS-DANLOS SYNDROME WITH PERIVENTRICULAR HETEROTOPIA CARNEY TRIAD MICROCEPHALY, PROGRESSIVE, WITH SEIZURES AND CEREBRAL AND CEREBELLAR ATROPHY; MSCCA NEUTROPENIA, SEVERE CONGENITAL, 7, AUTOSOMAL RECESSIVE; SCN7 RETINITIS PIGMENTOSA 50; RP50