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GENATLAS PHENOTYPE
last update : 07-06-2011
Symbol CMD1R
Location 15q14
Name cardiomyopathy, dilated 1R
Other name(s) cardiomyopathy, dilated 1A, with conduction defect
Corresponding gene ACTC1
Other symbol(s) CMD1ACT
Main clinical features idiopathic dilated cardiomyopathy
Genetic determination autosomal dominant
Related entries including cardiomyopathy familial hypertrophic, and idiopathic restrictive cardiomyopathy in childhood (PMID: 18467357)
Function/system disorder cardiovascular
neuromuscular
Type disease
Gene product
Name actin, alpha, cardiac (ACTC)
Remark(s)