ORPHA:217613
Mitochondrial disease 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 | Mitochondrial disease with dilated cardiomyopathy | |
| fr | Maladie mitochondriale avec cardiomyopathie dilatée | |
| de | Mitochondriale Krankheit mit dilatativer Kardiomyopathie | |
| es | Enfermedad mitocondrial con miocardiopatía dilatada | |
| it | Malattia mitocondriale con cardiomiopatia dilatativa | |
| nl | Mitochondriale ziekte met gedilateerde cardiomyopathie | |
| pt | Doença mitocondrial com miocardiopatia dilatada | |
| pl | Choroba mitochondrialna z kardiomiopatią rozstrzeniową | |
| cs | Mitochondriální choroba s dilatační kardiomyopatií | |
| uk | Мітохондріальна хвороба з дилатаційною кардіоміопатією | |
| zh | 线粒体疾病伴扩张型心肌病 | |
| tr | Dilate kardiyomiyopatili mitokondriyal hastalık |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 16335 | E | validated | |
| UMLS | C5680874 | 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
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Genes
0 directOrphanet records no gene directly on this code.
5
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/217613
- This record as JSON: /data/d/217613.json