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hypertrophic cardiomyopathy 8 | RareConnect | RareConnect.io

/familial hypertrophic cardiomyopathy

/hypertrophic cardiomyopathy 8

hypertrophic cardiomyopathy 8

Rare Disease

MONDO:0012111

Also Known As

MYL3 hypertrophic cardiomyopathycardiomyopathy hypertrophic mid-left ventricular chamber type 1cardiomyopathy, familial hypertrophic, 8cardiomyopathy, familial hypertrophic, type 8cardiomyopathy, hypertrophic, 8hypertrophic cardiomyopathy 8hypertrophic cardiomyopathy caused by mutation in MYL3hypertrophic cardiomyopathy type 8CMH8cardiomyopathy, hypertrophic, mid-left ventricular chamber type, 1

Definition

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the MYL3 gene.

Patient-Friendly Information

Comprehensive, easy-to-understand information about this condition

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Associated Genes

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:608751 ↗

Related Diseases

hypertrophic cardiomyopathy 2

MONDO:0007266

hypertrophic cardiomyopathy 3

MONDO:0007267

hypertrophic cardiomyopathy 4

MONDO:0007268

Beckwith-Wiedemann syndrome

MONDO:0007534

myotonic dystrophy type 1

MONDO:0008056

hypertrophic cardiomyopathy 1

MONDO:0008647

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