Cardiomyopathy, Familial Hypertrophic, 10 (CMH10)

Cardiomyopathy, Familial Hypertrophic, 10(来自ICD-11)

别称:

Hypertrophic Cardiomyopathy 10

Cmh10

Familial Hypertrophic Cardiomyopathy with Mid-Left Ventricular Chamber Type 2

Cardiomyopathy, Hypertrophic, Mid-Left Ventricular Chamber Type, 2

Cardiomyopathy, Hypertrophic, Familial, Type 10

Cardiomyopathy, Hypertrophic, 10

Mvc2

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Cardiomyopathy, Familial Hypertrophic, 10, also known as hypertrophic cardiomyopathy 10, is related to cardiomyopathy, familial hypertrophic, 1 and hypertrophic cardiomyopathy, and has symptoms including chest pain, dizziness and dyspnea. An important gene associated with Cardiomyopathy, Familial Hypertrophic, 10 is MYL2 (Myosin Light Chain 2), and among its related pathways/superpathways is Peptide hormone metabolism. Affiliated tissues include heart and skeletal muscle, and related phenotypes are hypertrophic cardiomyopathy and left ventricular hypertrophy

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