ORPHA:217619
Syndrome associated with dilated cardiomyopathy
- Type
- Category
- Group
- Group of disorders
- Status
- active
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.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Syndrome associated with dilated cardiomyopathy | |
| fr | Syndrome associé à une cardiomyopathie dilatée | |
| de | Seltenes Syndrom mit assoziierter dilatativer Kardiomyopathie | |
| es | Síndrome asociado a una miocardiopatía dilatada | |
| it | Sindrome associata a cardiomiopatia dilatativa | |
| nl | Syndroom geassocieerd met gedilateerde cardiomyopathie | |
| pt | Síndrome associado a miocardiopatia dilatada | |
| pl | Zespół z towarzyszącą kardiomiopatią rozstrzeniową | |
| cs | Syndrom asociovaný s dilatační kardiomyopatií | |
| uk | Синдром, повязаний з дилатаційною кардіоміопатією | |
| zh | 扩张型心肌病相关综合征 | |
| tr | Dilate kardiyomiyopati -ilişkili sendrom |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16337 | E | validated | |
| UMLS | C5680876 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:217607Familial dilated cardiomyopathy
rare cardiac diseases; rare genetic diseases - ORPHA:506225Rare disorder potentially indicated for heart transplant
rare transplant-related disorders
Children (15):
- ORPHA:16061p36 deletion syndrome
- ORPHA:64Alström syndrome
- ORPHA:1345Cardiomyopathy-cataract-hip spine disease syndrome
- ORPHA:65282Carvajal syndrome
- ORPHA:66634Dilated cardiomyopathy with ataxia
- ORPHA:2229Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
- ORPHA:476096Erythrokeratodermia-cardiomyopathy syndrome
- ORPHA:168796Heart-hand syndrome, Slovenian type
- ORPHA:79159Isobutyryl-CoA dehydrogenase deficiency
- ORPHA:73224Kidney tubulopathy-dilated cardiomyopathy syndrome
- ORPHA:59306McLeod neuroacanthocytosis syndrome
- ORPHA:2515Microcephaly-cardiomyopathy syndrome
- ORPHA:2663Nathalie syndrome
- ORPHA:217622Sensorineural deafness with dilated cardiomyopathy
- ORPHA:1493Vici syndrome
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/217619
- This record as JSON: /data/d/217619.json