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OMIM

Gene

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GENATLAS PHENOTYPE

last update : 21/10/2008

Symbol	CMD1M
Location	11p15.1
Name	cardiomyopathy, dilated 1M
Corresponding gene	CSRP3
Main clinical features	chamber dilation, thin ventricular walls, decreased contractility and impaired relaxation also hypertrophic cardiomyopathy, pronounced hypertrophy with an onset of symptoms in young adulthood, associated or not with typical myofibrillar myopathy
Genetic determination
Function/system disorder	cardiovascular
Type	disease

Gene product

Name	cysteine and glycine-rich protein 3 (cardiac LIM protein)

Remark(s)