Cardiomyopathy

0001638

Normal Case/Contol

GWAS of 0001638

Sibling Case/Control

No sibling GWAS available 0001638

Statistics

Case Control
12289 447905

Phenotype Definition

A myocardial disorder in which the heart muscle is structurally and functionally abnormal, in the absence of coronary artery disease, hypertension, valvular disease and congenital heart disease sufficient to cause the observed myocardial abnormality. [HPO:probinson, PMID:17916581]


Top SNP Information

Associated Diseases

ID Name Top Correlation
ICD: I214 Acute subendocardial myocardial infarction 2/20
ICD: I319 Disease of pericardium, unspecified 2/20
ICD: I422 Other hypertrophic cardiomyopathy 2/20
ICD: M548 Other dorsalgia 1/20
ICD: M5490 Dorsalgia, unspecified (Multiple sites in spine) 1/20
ICD: M5499 Dorsalgia, unspecified (Site unspecified) 2/20