ORPHA:716459
Rare disorder with progressive retinal vasculopathy as a major feature
Synonyms: Rare syndromic progressive retinal vasculopathy
- 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
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare disorder with progressive retinal vasculopathy as a major feature | Rare syndromic progressive retinal vasculopathy |
| fr | Maladie rare avec vasculopathie rétinienne progressive comme manifestation majeure | Maladie rare avec vasculopathie rétinienne progressive syndromique |
| de | Seltene Störung mit progredienter retinaler Vaskulopathie als Hauptmerkmal | Seltene syndromale progrediente retinale Vaskulopathie |
| es | Trastorno raro con vasculopatía retiniana progresiva como característica principal | Vasculopatía retiniana progresiva sindrómica rara |
| it | Malattia rara con vasculopatia retinica progressiva come caratteristica principale | Vasculopatia retinica progressiva sindromica rara |
| nl | Zeldzame aandoening met progressieve retinale vasculopathie als een hoofdkenmerk | Zeldzame syndromale progressieve retinale vasculopathie |
| pt | Rare disorder with progressive retinal vasculopathy as a major feature | |
| pl | Rzadkie zaburzenie z postępującą waskulopatią siatkówki jako dominującą cechą | = en |
| cs | Rare disorder with progressive retinal vasculopathy as a major feature | = en |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:716455Rare progressive retinal vasculopathy
rare ophthalmic disorders
Children (14):
- ORPHA:136CADASIL
- ORPHA:190Coats disease
- ORPHA:313838Coats plus syndrome
- ORPHA:40923Eales disease
- ORPHA:209943IRVAN syndrome
- ORPHA:464Incontinentia pigmenti
- ORPHA:649Norrie disease
- ORPHA:2788Osteoporosis-pseudoglioma syndrome
- ORPHA:247691Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations
- ORPHA:90050Retinopathy of prematurity
- ORPHA:2715Severe oculo-renal-cerebellar syndrome
- ORPHA:506307Stromme syndrome
- ORPHA:3205Sturge-Weber syndrome
- ORPHA:838Susac syndrome
4
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/716459
- This record as JSON: /data/d/716459.json