ORPHA:167848
Rare 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 | Rare cardiomyopathy | |
| fr | Cardiomyopathie rare | |
| de | Seltene Kardiomyopathie | |
| es | Miocardiopatía rara | Cardiomiopatía rara |
| it | Cardiomiopatia rara | |
| nl | Zeldzame cardiomyopathie | |
| pt | Cardiomiopatia | |
| pl | Kardiomiopatia rzadka | |
| cs | Kardiomyopatie | |
| uk | Рідкісна кардіоміопатія | |
| zh | 罕见心肌病 | |
| tr | Nadir kardiyomiyopati |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 4994 | E | validated | |
| MeSH | D009202 | E | validated | |
| UMLS | C5680467 | E | validated | |
| MedDRA | 10007636 | 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 (1):
- ORPHA:97929Rare cardiac disease
rare cardiac diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:90022OBSOLETE: Cardiomyopathy-renal anomalies syndrome referred to · inactive
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/167848
- This record as JSON: /data/d/167848.json