ORPHA:217607
Familial 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Familial dilated cardiomyopathy | |
| fr | Cardiomyopathie dilatée familiale | |
| de | Kardiomyopathie, dilatative, familiäre Form | |
| es | Miocardiopatía dilatada familiar | |
| it | Cardiomiopatia dilatativa familiare | |
| nl | Familiale gedilateerde cardiomyopathie | |
| pt | Miocardiopatia dilatada, familiar | |
| pl | Rodzinna kardiomiopatia rozstrzeniowa | |
| cs | Familiární dilatační kardiomyopatie | |
| uk | Сімейна дилатаційна кардіоміопатія | |
| zh | 家族性扩张型心肌病 | |
| tr | Ailesel dilate kardiyomiyopati |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0016333 | E | validated | |
| MONDO | 16333 | E | validated | |
| MeSH | C536231 | E | validated | |
| UMLS | C0340427 | E | validated | |
| MedDRA | 10088172 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (2):
- ORPHA:217604Dilated cardiomyopathy
rare cardiac diseases - ORPHA:98054Rare genetic cardiac disease
rare genetic diseases
Children (10):
- ORPHA:371176Congenital disorder of glycosylation with dilated cardiomyopathy
- ORPHA:34587Danon disease
- ORPHA:300751Familial dilated cardiomyopathy with conduction defect due to LMNA mutation
- ORPHA:154Familial isolated dilated cardiomyopathy
- ORPHA:217616Fatty acid oxidation and ketogenesis disorder with dilated cardiomyopathy
- ORPHA:367Glycogen storage disease due to glycogen branching enzyme deficiency
- ORPHA:2119HEC syndrome
- ORPHA:217613Mitochondrial disease with dilated cardiomyopathy
- ORPHA:217610Neuromuscular disease with dilated cardiomyopathy
- ORPHA:217619Syndrome associated with dilated cardiomyopathy
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
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/217607
- This record as JSON: /data/d/217607.json