ORPHA:217632
Restrictive 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 | Restrictive cardiomyopathy | |
| fr | Cardiomyopathie restrictive | |
| de | Kardiomyopathie, restriktive | |
| es | Miocardiopatía restrictiva | Cardiomiopatía restrictiva |
| it | Cardiomiopatia restrittiva | |
| nl | Restrictieve cardiomyopathie | |
| pt | Miocardiopatia restritiva | |
| pl | Kardiomiopatia restrykcyjna | |
| cs | Restriktivní kardiomyopatie | |
| uk | Рестриктивна кардіоміопатія | |
| zh | 限制型心肌病 | |
| tr | Restriktif kardiyomiyopati |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | BC43.2 | E | specific | validated |
| MONDO | 0005201 | E | validated | |
| MONDO | 5201 | E | validated | |
| MeSH | D002313 | E | validated | |
| UMLS | C0007196 | E | validated | |
| MedDRA | 10038748 | 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:167848Rare cardiomyopathy
rare cardiac diseases
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.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/217632
- This record as JSON: /data/d/217632.json