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hypertrophic cardiomyopathy 25 | RareConnect | RareConnect.io

/neuromuscular disease caused by qualitative or quantitative defects of telethonin

/familial dilated cardiomyopathy

/familial hypertrophic cardiomyopathy

/hypertrophic cardiomyopathy 25

hypertrophic cardiomyopathy 25

Rare Disease

MONDO:0011843

Also Known As

CMH25TCAP hypertrophic cardiomyopathyTcap hypertrophic cardiomyopathycardiomyopathy familial hypertrophic 25cardiomyopathy, familial hypertrophic, type 25cardiomyopathy, hypertrophic, 25hypertrophic cardiomyopathy caused by mutation in TCAPhypertrophic cardiomyopathy type 25cardiomyopathy, familial hypertrophic, 25

Definition

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TCAP 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:607487 ↗

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