ORPHA:3421
Cerebroretinal vasculopathy
inactive · moved to ORPHA:247691Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
Synonyms: CRV · Grand-Kaine-Fulling syndrome
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Cerebroretinal vasculopathy | CRV · Grand-Kaine-Fulling syndrome |
| fr | Vasculopathie cérébro-rétinienne | CRV · Syndrome de Grand-Kaine-Fulling |
| de | Vaskulopathie, zerebro-retinale | Grand-Kaine-Fulling-Syndrom |
| es | Vasculopatía cerebrorretiniana | Síndrome de Grand-Kaine-Fulling |
| it | Vasculopatia cerebroretinica | Sindrome di Grand-Kaine-Fulling |
| nl | Cerebroretinale vasculopathie | CRV · Syndroom van Grand-Kaine-Fulling |
| pt | Vasculopatia cerebro-retiniana | CRV · Síndrome Grand-Kaine-Fulling |
| pl | Naczyniopatia mózgowo-siatkówkowa | CRV · Zespół Granda, Kaine i Fullinga |
| cs | Cerebroretinální vaskulopatie | CRV · Grandův-Kaineho-Fullingův syndrom · Grand-Kaine-Fullingův syndrom |
| uk | Цереброретинальна васкулопатія | CRV · Синдром Гранд-Кейна-Фуллінг |
| zh | 脑视网膜血管病 | Grand-Kaine-Fulling 综合征 |
| tr | Serebroretinal vaskülopati | CRV · Grand-Kaine-Fulling sendromu |
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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/3421
- This record as JSON: /data/d/3421.json