{"disease":{"id":"OMIM:613690","name":"Cardiomyopathy, familial hypertrophic, 7","mondoId":"MONDO:0013369","description":"Any hypertrophic cardiomyopathy in which the cause of the disease is a mutation in the TNNI3 gene."},"categories":{"Clinical course":[{"id":"HP:0003581","name":"Adult onset","metadata":{"sex":"","onset":"","frequency":"6/6","sources":["PMID:11815426"]},"category":"Clinical course"}],"Cardiovascular":[{"id":"HP:0001716","name":"Wolff-Parkinson-White syndrome","metadata":{"sex":"","onset":"","frequency":"3/6","sources":["PMID:9241277"]},"category":"Cardiovascular"},{"id":"HP:0031992","name":"Apical hypertrophic cardiomyopathy","metadata":{"sex":"","onset":"","frequency":"3/6","sources":["PMID:9241277"]},"category":"Cardiovascular"},{"id":"HP:0005110","name":"Atrial fibrillation","metadata":{"sex":"","onset":"","frequency":"Occasional","sources":["OMIM:613690"]},"category":"Cardiovascular"},{"id":"HP:0001714","name":"Ventricular hypertrophy","metadata":{"sex":"","onset":"","frequency":"","sources":["OMIM:613690"]},"category":"Cardiovascular"},{"id":"HP:0001639","name":"Hypertrophic cardiomyopathy","metadata":{"sex":"","onset":"","frequency":"2/2","sources":["PMID:11815426"]},"category":"Cardiovascular"}],"Inheritance":[{"id":"HP:0000006","name":"Autosomal dominant inheritance","metadata":{"sex":"","onset":"","frequency":"","sources":["PMID:9241277"]},"category":"Inheritance"}]},"genes":[{"id":"NCBIGene:7137","name":"TNNI3"}],"medicalActions":[]}