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Up to: Hypertrophic cardiomyopathy · Familial cardiomyopathy
Familial hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy caused by mutations in the genes encoding components of the sarcomere, in the absence of predisposing conditions.
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Noonan syndrome and Noonan-related syndrome 1 trial · 29 incl. sub-types Sub-types →
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Beckwith-Wiedemann syndrome 6 trials Sub-types →
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Dilated cardiomyopathy 1C 1 trial
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46,XY complete gonadal dysgenesis 0 trials · 1 incl. sub-types Sub-types →
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Dilated cardiomyopathy 1KK 0 trials
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Hypertrophic cardiomyopathy 1 0 trials
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Hypertrophic cardiomyopathy 10 0 trials
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Hypertrophic cardiomyopathy 25 0 trials
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