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hypertrophic cardiomyopathy 2 | RareConnect | RareConnect.io

/familial hypertrophic cardiomyopathy

/hypertrophic cardiomyopathy 2

hypertrophic cardiomyopathy 2

Rare Disease

MONDO:0007266

Also Known As

CMH2TNNT2 hypertrophic cardiomyopathycardiomyopathy familial hypertrophic 2cardiomyopathy, familial hypertrophic, type 2cardiomyopathy, hypertrophic, 2familial hypertrophic cardiomyopathy type 2hypertrophic cardiomyopathy 2hypertrophic cardiomyopathy caused by mutation in TNNT2hypertrophic cardiomyopathy type 2cardiomyopathy, familial hypertrophic, 2

Definition

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TNNT2 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:115195 ↗

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