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hypertrophic cardiomyopathy 3 | RareConnect | RareConnect.io

/familial hypertrophic cardiomyopathy

/hypertrophic cardiomyopathy 3

hypertrophic cardiomyopathy 3

Rare Disease

MONDO:0007267

Also Known As

CMH3TPM1 hypertrophic cardiomyopathycardiomyopathy familial hypertrophic 3cardiomyopathy, familial hypertrophic, type 3cardiomyopathy, hypertrophic, 3hypertrophic cardiomyopathy 3hypertrophic cardiomyopathy caused by mutation in TPM1hypertrophic cardiomyopathy type 3cardiomyopathy, familial hypertrophic, 3

Definition

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TPM1 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:115196 ↗

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