{"orpha":217595,"name":"Syndrome associated with hypertrophic cardiomyopathy","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-217595/","orphanet_url":"https://www.orpha.net/en/disease/detail/217595","names":{"fr":{"name":"Syndrome associé à une cardiomyopathie hypertrophique"},"de":{"name":"Seltenes Syndrom mit assoziierter hypertropher Kardiomyopathie"},"es":{"name":"Síndrome asociado a una miocardiopatía hipertrófica"},"it":{"name":"Sindrome associata a cardiomiopatia ipertrofica"},"nl":{"name":"Syndroom geassocieerd met hypertrofische cardiomyopathie"},"pt":{"name":"Síndrome associado a miocardiopatia hipertrófica"},"pl":{"name":"Zespół z towarzyszącą kardiomiopatią przerostową"},"cs":{"name":"Syndrom asociovaný s hypertrofickou kardiomyopatií"},"uk":{"name":"Синдром, повязаний з гіпертрофічною кардіоміопатією"},"zh":{"name":"肥厚型心肌病相关综合征"},"tr":{"name":"Hipertrofik kardiyomiyopati -ilişkili sendrom"}},"xrefs":[{"source":"UMLS","code":"C5680881","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97929,"name":"Rare cardiac disease"},"parents":[{"orpha":99739,"name":"Rare familial disorder with hypertrophic cardiomyopathy","classifications":[146,156,233]}],"children":[{"orpha":693647,"name":"Agammaglobulinemia-early-onset hypertrophic cardiomyopathy-neutropenia syndrome","type":"Disease"},{"orpha":399058,"name":"Alpha-B crystallin-related late-onset myopathy","type":"Disease"},{"orpha":116,"name":"Beckwith-Wiedemann syndrome","type":"Malformation syndrome"},{"orpha":1340,"name":"Cardiofaciocutaneous syndrome","type":"Malformation syndrome"},{"orpha":91130,"name":"Cardiomyopathy-hypotonia-lactic acidosis syndrome","type":"Disease"},{"orpha":3071,"name":"Costello syndrome","type":"Malformation syndrome"},{"orpha":98909,"name":"Desminopathy","type":"Disease"},{"orpha":95,"name":"Friedreich ataxia","type":"Disease"},{"orpha":726824,"name":"Hepatorenocardiac degenerative fibrosis","type":"Disease"},{"orpha":648,"name":"Noonan syndrome","type":"Malformation syndrome"},{"orpha":500,"name":"Noonan syndrome with multiple lentigines","type":"Malformation syndrome"},{"orpha":363972,"name":"Noonan syndrome-like disorder with juvenile myelomonocytic leukemia","type":"Malformation syndrome"},{"orpha":2701,"name":"Noonan syndrome-like disorder with loose anagen hair","type":"Malformation syndrome"},{"orpha":228012,"name":"Progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome","type":"Disease"},{"orpha":273,"name":"Steinert myotonic dystrophy","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}