Cardiomyopathy, Dilated, 1a (CMD1A)

Cardiomyopathy, Dilated, 1a(来自ICD-11)

别称:

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

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

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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