Cardiomyopathy, Dilated, 1v; Cmd1v

Clinical Features

Phenotypes and symptoms related to Cardiomyopathy, Dilated, 1v; Cmd1v

  • Cardiomyopathy
  • Congestive heart failure
  • Dementia
  • Dilated cardiomyopathy
  • Syncope
  • Abnormality of the cardiovascular system
  • Myocardial infarction
  • Bundle branch block
  • Abnormal EKG
  • Myocardial fibrosis

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, Dilated, 1v; Cmd1v Recommended genes panels

Panel Name, Specifity and genes Tested/covered
ADmark® PSEN2 DNA Sequencing Test.

By Athena Diagnostics Inc (United States).

PSEN2
Specificity
100 %
Genes
100 %
ADmark® Early Onset Alzheimer's Evaluation.

By Athena Diagnostics Inc (United States).

APP, PSEN1, PSEN2
Specificity
34 %
Genes
100 %
Dementia.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University (United States).

SORL1, TARDBP, VCP, FIG4, OPTN, TREM2, CSF1R, CHMP2B, DCTN1, C9orf72, FUS, ALS2, SETX, GRN, ANG, APOE, APP, MAPT, PRNP, PSEN1 , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
100 %
APOE, APP, PSEN1, PSEN2. NextGeneDx.Complete sequencing by NGS.

By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).

APOE, APP, PSEN1, PSEN2
Specificity
25 %
Genes
100 %
PSEN2. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).

PSEN2
Specificity
100 %
Genes
100 %
ACTC1, DES, LDB3, MYH6, PSEN1, PSEN2, TCAP, TNNC1, TPM1, VCL. NextGeneDx.Complete sequencing by NGS.

By Instituto de Medicina Genomica Instituto de Medicina Genomica (Spain).

TCAP, TNNC1, TPM1, VCL, ACTC1, LDB3, DES, MYH6, PSEN1, PSEN2
Specificity
10 %
Genes
100 %
Alzheimer disease type 4 (sequence analysis of PSEN2 gene).

By CGC Genetics (Portugal).

PSEN2
Specificity
100 %
Genes
100 %
Alzheimer disease types 1, 3 and 4 (sequence analysis of APP, PSEN1 and PSEN2 genes).

By CGC Genetics (Portugal).

APP, PSEN1, PSEN2
Specificity
34 %
Genes
100 %

You can get up to 62 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM MESH Genetic Syndrome Finder

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like GLYCOGEN STORAGE DISEASE III; GSD3 AGENESIS OF THE CORPUS CALLOSUM WITH PERIPHERAL NEUROPATHY; ACCPN MOYAMOYA DISEASE 6 WITH ACHALASIA; MYMY6 KEPPEN-LUBINSKY SYNDROME; KPLBS PULMONARY HYPERTENSION, PRIMARY, 1; PPH1 HYPERINSULINISM DUE TO SHORT CHAIN 3-HYDROXYLACYL-COA DEHYDROGENASE DEFICIENCY