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Familial hypertrophic cardiomyopathy

MONDO:0024573

Hypertrophic cardiomyopathy caused by mutations in the genes encoding components of the sarcomere, in the absence of predisposing conditions.

Also known as: cardiomyopathy, familial hypertrophic, familial hypertrophic cardiomyopathy, familila or idiopathic hypertrophic obstructive cardiomyopathy, hereditary hypertrophic cardiomyopathy, hypertrophic familial cardiomyopathy

89 clinical trials for this condition and its sub-types.

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Sub-types

Myotonic dystrophy type 1 (44) Noonan syndrome (20) Beckwith-Wiedemann syndrome (6) Cardiofaciocutaneous syndrome (6) Costello syndrome (6) Legius syndrome (5) Noonan syndrome with multiple lentigines (3) Noonan syndrome 3 (2) Cardiofaciocutaneous syndrome 1 (1) Congenital-onset Steinert myotonic dystrophy (1) Dilated cardiomyopathy 1C (1) Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (1) Multiple acyl-CoA dehydrogenase deficiency (1) Noonan syndrome 5 (1) Very long chain acyl-CoA dehydrogenase deficiency (1) 46,XY complete gonadal dysgenesis (0) 46,XY disorder of sex development due to testicular 17,20-desmolase deficiency (0) 46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome (0) 46,XY sex reversal 1 (0) 46,XY sex reversal 10 (0)

Broader categories

Cardiovascular disorder (1051) Disease (680) Heart disorder (300) Musculoskeletal system disorder (207) Hereditary disease (176) Cardiomyopathy (144) Hypertrophic cardiomyopathy (112) Muscle tissue disorder (56) Intrinsic cardiomyopathy (16) Human disease (14)
Trials to join now! 43 Not yet recruiting 7 Not yet finished but already full! 20 Completed 17 Terminated 2
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