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hypertrophic cardiomyopathy 12 | RareConnect | RareConnect.io

/familial hypertrophic cardiomyopathy

/hypertrophic cardiomyopathy 12

hypertrophic cardiomyopathy 12

Rare Disease

MONDO:0012804

Also Known As

CMH12CSRP3 hypertrophic cardiomyopathycardiomyopathy familial hypertrophic 12cardiomyopathy, familial hypertrophic, type 12cardiomyopathy, hypertrophic, 12hypertrophic cardiomyopathy 12hypertrophic cardiomyopathy caused by mutation in CSRP3hypertrophic cardiomyopathy type 12cardiomyopathy, familial hypertrophic, 12

Definition

Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the CSRP3 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:612124 ↗

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MONDO:0007266

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MONDO:0008647

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