ORPHA:217635
Familial 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 | Familial restrictive cardiomyopathy | |
| fr | Cardiomyopathie familiale restrictive | |
| de | Kardiomyopathie, restriktive, familiäre Form | |
| es | Miocardiopatía restrictiva familiar | Cardiomiopatía restrictiva familiar |
| it | Cardiomiopatia restrittiva familiare | |
| nl | Familiale restrictieve cardiomyopathie | |
| pt | Miocardiopatia restritiva familiar | |
| pl | Rodzinna kardiomiopatia restrykcyjna | |
| cs | Familiární restriktivní kardiomyopatie | |
| uk | Сімейна рестриктивна кардіоміопатія | |
| zh | 家族性限制型心肌病 | |
| tr | Ailesel restriktif kardiyomiyopati |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0016340 | E | validated | |
| MONDO | 16340 | E | validated | |
| UMLS | C0340429 | 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:98054Rare genetic cardiac disease
rare genetic diseases - ORPHA:217632Restrictive 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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/217635
- This record as JSON: /data/d/217635.json