{"orpha":217619,"name":"Syndrome associated with dilated 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-217619/","orphanet_url":"https://www.orpha.net/en/disease/detail/217619","names":{"fr":{"name":"Syndrome associé à une cardiomyopathie dilatée"},"de":{"name":"Seltenes Syndrom mit assoziierter dilatativer Kardiomyopathie"},"es":{"name":"Síndrome asociado a una miocardiopatía dilatada"},"it":{"name":"Sindrome associata a cardiomiopatia dilatativa"},"nl":{"name":"Syndroom geassocieerd met gedilateerde cardiomyopathie"},"pt":{"name":"Síndrome associado a miocardiopatia dilatada"},"pl":{"name":"Zespół z towarzyszącą kardiomiopatią rozstrzeniową"},"cs":{"name":"Syndrom asociovaný s dilatační kardiomyopatií"},"uk":{"name":"Синдром, повязаний з дилатаційною кардіоміопатією"},"zh":{"name":"扩张型心肌病相关综合征"},"tr":{"name":"Dilate kardiyomiyopati -ilişkili sendrom"}},"xrefs":[{"source":"MONDO","code":"16337","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680876","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97929,"name":"Rare cardiac disease"},"parents":[{"orpha":217607,"name":"Familial dilated cardiomyopathy","classifications":[146,156]},{"orpha":506225,"name":"Rare disorder potentially indicated for heart transplant","classifications":[233]}],"children":[{"orpha":1606,"name":"1p36 deletion syndrome","type":"Malformation syndrome"},{"orpha":64,"name":"Alström syndrome","type":"Disease"},{"orpha":1345,"name":"Cardiomyopathy-cataract-hip spine disease syndrome","type":"Disease"},{"orpha":65282,"name":"Carvajal syndrome","type":"Disease"},{"orpha":66634,"name":"Dilated cardiomyopathy with ataxia","type":"Disease"},{"orpha":2229,"name":"Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome","type":"Malformation syndrome"},{"orpha":476096,"name":"Erythrokeratodermia-cardiomyopathy syndrome","type":"Disease"},{"orpha":168796,"name":"Heart-hand syndrome, Slovenian type","type":"Malformation syndrome"},{"orpha":79159,"name":"Isobutyryl-CoA dehydrogenase deficiency","type":"Disease"},{"orpha":73224,"name":"Kidney tubulopathy-dilated cardiomyopathy syndrome","type":"Disease"},{"orpha":59306,"name":"McLeod neuroacanthocytosis syndrome","type":"Disease"},{"orpha":2515,"name":"Microcephaly-cardiomyopathy syndrome","type":"Malformation syndrome"},{"orpha":2663,"name":"Nathalie syndrome","type":"Malformation syndrome"},{"orpha":217622,"name":"Sensorineural deafness with dilated cardiomyopathy","type":"Disease"},{"orpha":1493,"name":"Vici syndrome","type":"Malformation syndrome"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}