Cardiomyopathy, Familial Hypertrophic, 8 (CMH8)

Cardiomyopathy, Familial Hypertrophic, 8(来自ICD-11)

别称:

Hypertrophic Cardiomyopathy 8

Cmh8

Familial Hypertrophic Cardiomyopathy with Mid-Left Ventricular Chamber Type 1

Cardiomyopathy, Hypertrophic, Mid-Left Ventricular Chamber Type, 1

Cardiomyopathy Hypertrophic Mid-Left Ventricular Chamber Type 1

Cardiomyopathy, Hypertrophic, Familial, Type 8

Cardiomyopathy, Hypertrophic, 8

Mvc1

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Cardiomyopathy, Familial Hypertrophic, 8, is also known as hypertrophic cardiomyopathy 8, and has symptoms including dyspnea on exertion An important gene associated with Cardiomyopathy, Familial Hypertrophic, 8 is MYL3 (Myosin Light Chain 3). Affiliated tissues include heart and skeletal muscle, and related phenotypes are congestive heart failure and hypertrophic cardiomyopathy

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