familial hypertrophic cardiomyopathy
MONDO:0024573Also known as: cardiomyopathy, familial hypertrophic, familial hypertrophic cardiomyopathy, familila or idiopathic hypertrophic obstructive cardiomyopathy, hereditary hypertrophic cardiomyopathy, hypertrophic familial cardiomyopathy
- MONDO:
- MONDO:0024573
- Orphanet:
- 155 ↗
Rare disease44 associated genes
Description
Hypertrophic cardiomyopathy caused by mutations in the genes encoding components of the sarcomere, in the absence of predisposing conditions.
Associated genes
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