ORPHA:99986
OBSOLETE: Familial restrictive cardiomyopathy type 2
inactive · referred to ORPHA:75249Familial isolated restrictive cardiomyopathy
- Type
- Etiological subtype
- Group
- Subtype of disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Familial isolated restrictive cardiomyopathy
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Familial restrictive cardiomyopathy type 2 | |
| fr | OBSOLETE : Cardiomyopathie restrictive familiale type 2 | |
| de | OBSOLET: Kardiomyopathie, restriktive, familiäre, Typ 2 | |
| es | OBSOLETO: Miocardiopatía restrictiva familiar tipo 2 | OBSOLETO: Cardiomiopatía restrictiva familiar tipo 2 |
| it | OBSOLETO: Cardiomiopatia restrittiva familiare, tipo 2 | |
| nl | OBSOLEET: Familiale restrictieve cardiomyopathie type 2 | |
| pt | OBSOLETO: Miocardiopatia restritiva, familiar, tipo 2 | |
| pl | NIEAKTUALNE: Rodzinna kardiomiopatia restrykcyjna typu 2 | |
| cs | NEAKTUÁLNÍ: Familiární restriktivní kardiomyopatie, typ 2 | |
| uk | ЗАСТАРІЛО: Сімейна рестриктивна кардіоміопатія, тип 2 | |
| zh | 弃用：家族性限制性心肌病2型 | |
| tr | Eski adı: ailesel restriktif kardiyomiyopati tip 2 |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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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/99986
- This record as JSON: /data/d/99986.json