{"orpha":506225,"name":"Rare disorder potentially indicated for heart transplant","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-506225/","orphanet_url":"https://www.orpha.net/en/disease/detail/506225","names":{"fr":{"name":"Maladie rare possiblement indiquée pour la transplantation cardiaque"},"de":{"name":"Seltene Erkrankung zur potentiellen Herz-Transplantation indiziert"},"es":{"name":"Trastorno raro potencialmente indicado para trasplante cardíaco"},"it":{"name":"Malattia rara con indicazione al trapianto cardiaco"},"nl":{"name":"Zeldzame aandoening mogelijk geïndiceerd voor harttransplantatie"},"pt":{"name":"Doença rara com potencial indicação para transplante cardíaco"},"pl":{"name":"Choroba rzadka będąca potencjalnym wskazaniem do przeszczepu serca"},"cs":{"name":"Vzácná porucha indikovaná k transplantaci srdce"},"uk":{"name":"Рідкісне захворювання, яке може бути показанням для трансплантації серця"},"zh":{"name":"可能适用于心脏移植的罕见疾病"},"tr":{"name":"Potansiyel olarak kalp nakli için endike olan nadir hastalık"}},"xrefs":[{"source":"UMLS","code":"C5681216","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":565779,"name":"Rare disorder potentially indicated for transplant or complication after transplantation"},"parents":[{"orpha":506207,"name":"Rare disorder potentially indicated for transplant","classifications":[233]}],"children":[{"orpha":85451,"name":"ATTRV122I amyloidosis","type":"Clinical subtype"},{"orpha":371176,"name":"Congenital disorder of glycosylation with dilated cardiomyopathy","type":"Category"},{"orpha":2022,"name":"Endocardial fibroelastosis","type":"Disease"},{"orpha":300751,"name":"Familial dilated cardiomyopathy with conduction defect due to LMNA mutation","type":"Disease"},{"orpha":154,"name":"Familial isolated dilated cardiomyopathy","type":"Disease"},{"orpha":75249,"name":"Familial isolated restrictive cardiomyopathy","type":"Disease"},{"orpha":217616,"name":"Fatty acid oxidation and ketogenesis disorder with dilated cardiomyopathy","type":"Category"},{"orpha":367,"name":"Glycogen storage disease due to glycogen branching enzyme deficiency","type":"Disease"},{"orpha":247,"name":"Inherited arrhythmogenic cardiomyopathy","type":"Clinical group"},{"orpha":217638,"name":"Lysosomal disease with restrictive cardiomyopathy","type":"Category"},{"orpha":217613,"name":"Mitochondrial disease with dilated cardiomyopathy","type":"Category"},{"orpha":217610,"name":"Neuromuscular disease with dilated cardiomyopathy","type":"Category"},{"orpha":324767,"name":"Non-familial rare disease with dilated cardiomyopathy","type":"Category"},{"orpha":563,"name":"Peripartum cardiomyopathy","type":"Disease"},{"orpha":217569,"name":"Rare hypertrophic cardiomyopathy","type":"Category"},{"orpha":217619,"name":"Syndrome associated with dilated cardiomyopathy","type":"Category"},{"orpha":692305,"name":"Triglyceride deposit cardiomyovasculopathy","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}