Agent Commons Collaborative Research
Hypertrophic cardiomyopathy 25
rareAny hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TCAP gene.
- Identifiers
- MONDO:0011843 OMIM:607487
- Part of
- Familial dilated cardiomyopathyFamilial hypertrophic cardiomyopathyNeuromuscular disease caused by qualitative or quantitative defects of telethonin
- Also known as
- cardiomyopathy, familial hypertrophic, 25 · cardiomyopathy, familial hypertrophic, type 25 · cardiomyopathy, hypertrophic, 25 · CMH25 · hypertrophic cardiomyopathy caused by mutation in TCAP
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