Cardiomyopathy, Familial Hypertrophic, 1 (CMH1)

Alias:

Familial Hypertrophic Cardiomyopathy

Asymmetric Septal Hypertrophy

Hypertrophic Cardiomyopathy 1

Hypertrophic Cardiomyopathy 19

Cmh1

Hypertrophic Subaortic Stenosis, Idiopathic

Cardiomyopathy, Hypertrophic, 1, Digenic

Cardiomyopathy, Hypertrophic, Familial

Cardiomyopathy, Familial Hypertrophic

Ventricular Hypertrophy, Hereditary

Hereditary Ventricular Hypertrophy

Hypertrophic Cardiomyopathy

Cmh

Ash

Hcm

Cardiomyopathy, Hypertrophic, Familial, Type 1

Idiopathic Hypertrophic Subaortic Stenosis

Cardiomyopathy, Familial Hypertrophic 1

Familial Asymmetric Septal Hypertrophy

Heritable Hypertrophic Cardiomyopathy

Cardiomyopathy, Hypertrophic, 1

Subaortic Hypertrophic Stenosis

Brock's Disease

Fhc

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Cardiomyopathy, Familial Hypertrophic, 1, also known as familial hypertrophic cardiomyopathy, is related to cardiomyopathy, familial hypertrophic, 25 and cardiomyopathy, familial hypertrophic, 11. An important gene associated with Cardiomyopathy, Familial Hypertrophic, 1 is MYH7 (Myosin Heavy Chain 7), and among its related pathways/superpathways are PAK Pathway and Sweet Taste Signaling. The drugs Ethanol and Metoprolol have been mentioned in the context of this disorder. Affiliated tissues include heart and skeletal muscle, and related phenotypes are congestive heart failure and arrhythmia

Related ID：

MALACARDS：CRD086

OMIM：192600

MESH：D024741