Results for "desmin-associated restrictive cardiomyopathy.": 11 genes

Name

CMR1A Gene

cardiomyopathy, restrictive 1A (autosomal dominant)

RCM2 Gene

cardiomyopathy, familial restrictive, 2

CMR2A Gene

cardiomyopathy, restrictive 2A (autosomal recessive)

CMR3A Gene

cardiomyopathy, restrictive 3A (X-linked)

DES Gene

desmin

This gene encodes a muscle-specific class III intermediate filament. Homopolymers of this protein form a stable intracytoplasmic filamentous network connecting myofibrils to each other and to the plasma membrane. Mutations in this gene are associated with desmin-related myopathy, a familial cardiac and skeletal myopathy (CSM), and with distal myopathies. [provided by RefSeq, Jul 2008]

CMD1K Gene

cardiomyopathy, dilated 1K (autosomal dominant)

CMD1H Gene

cardiomyopathy, dilated 1H (autosomal dominant)

CMD1F Gene

cardiomyopathy, dilated 1F (autosomal dominant)

CMD1B Gene

cardiomyopathy, dilated 1B (autosomal dominant)

CMD1Q Gene

cardiomyopathy, dilated 1Q (autosomal dominant)

CMH21 Gene

Cardiomyopathy, familial hypertrophic, 21