Cardiomyopathy, Dilated, 1a (CMD1A)
Alias:
Dilated Cardiomyopathy 1a
Cmd1a
Cardiomyopathy, Familial Idiopathic
Cdcd1
Familial Dilated Cardiomyopathy with Conduction Defect Due to Lmna Mutation
Congenital Muscular Dystrophy Due to Laminin Alpha2 Deficiency
Laminin Subunit Alpha 2-Related Congenital Muscular Dystrophy
Cardiomyopathy, Dilated, with Conduction Defect 1
Merosin-Negative Congenital Muscular Dystrophy
Congenital Muscular Dystrophy Type 1a
Cardiomyopathy, Idiopathic Dilated
Cardiomyopathy, Congestive
Mdc1a
Cardiomyopathy Dilated with Conduction Defect Type 1
Dilated Cardiomyopathy with Conduction Defect 1
Muscular Dystrophy Congenital, Merosin Negative
Cardiomyopathy Dilated with Conduction Defect 1
Idiopathic Dilated Cardiomyopathy
Cardiomyopathy, Dilated, Type 1a
Cardiomyopathy, Dilated, 1a, also known as dilated cardiomyopathy 1a, is related to familial isolated dilated cardiomyopathy and cardiomyopathy, dilated, 1e. An important gene associated with Cardiomyopathy, Dilated, 1a is LMNA (Lamin A/C), and among its related pathways/superpathways are Striated muscle contraction pathway and Familial partial lipodystrophy. The drugs Doxazosin and Metoprolol have been mentioned in the context of this disorder. Affiliated tissues include heart and bone marrow, and related phenotypes are hypotonia and muscle weakness
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