{"disease":{"id":"OMIM:607487","name":"Cardiomyopathy, familial hypertrophic, 25","mondoId":"MONDO:0011843","description":"Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TCAP gene."},"categories":{"Clinical course":[{"id":"HP:0003581","name":"Adult onset","metadata":{"sex":"","onset":"","frequency":"2/2","sources":["PMID:15582318"]},"category":"Clinical course"}],"Cardiovascular":[{"id":"HP:0001639","name":"Hypertrophic cardiomyopathy","metadata":{"sex":"","onset":"","frequency":"2/2","sources":["PMID:15582318"]},"category":"Cardiovascular"},{"id":"HP:0001712","name":"Left ventricular hypertrophy","metadata":{"sex":"","onset":"","frequency":"2/2","sources":["PMID:15582318"]},"category":"Cardiovascular"},{"id":"HP:0001716","name":"Wolff-Parkinson-White syndrome","metadata":{"sex":"","onset":"","frequency":"1/2","sources":["PMID:15582318"]},"category":"Cardiovascular"}],"Inheritance":[{"id":"HP:0000006","name":"Autosomal dominant inheritance","metadata":{"sex":"","onset":"","frequency":"","sources":["PMID:15582318"]},"category":"Inheritance"}]},"genes":[{"id":"NCBIGene:8557","name":"TCAP"}],"medicalActions":[]}