ORPHA:717324
Rare genetic isolated progressive generalized retinal disorder
Synonyms: Non-syndromic inherited retinal dystrophy · Non-syndromic IRD
- 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 genetic isolated progressive generalized retinal disorder | Non-syndromic inherited retinal dystrophy · Non-syndromic IRD |
| fr | Maladie génétique rare isolée rétinienne progressive généralisée | Dystrophie héréditaire de la rétine non syndromique |
| de | Seltene genetische isolierte progrediente generalisierte Retinopathie | Nicht-syndromale hereditäre Netzhautdystrophie |
| es | Trastorno retiniano generalizado progresivo aislado genético raro | Distrofia retiniana hereditaria no sindrómica · DRH no sindrómica |
| it | Retinopatia genetica rara progressiva generalizzata isolata | IRD non sindromica · Distrofia retinica ereditaria non sindromica |
| nl | Zeldzame genetische geïsoleerde progressieve gegeneraliseerde aandoening van retina | Niet-syndromale erfelijke retinadystrofie · Niet-syndromale IRD · Zeldzame genetische geïsoleerde progressieve gegeneraliseerde aandoening van netvlies |
| pt | Rare genetic isolated progressive generalized retinal disorder | |
| pl | Rzadkie genetycznie uwarunkowane postępujące uogólnione zaburzenie dotyczące siatkówki | = en |
| cs | Rare genetic isolated progressive generalized retinal disorder | = 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 (2):
- ORPHA:717321Rare genetic progressive generalized retinal disorder
rare genetic diseases - ORPHA:716410Rare isolated progressive generalized retinal disorder
rare ophthalmic disorders
Children (15):
- ORPHA:139455Autosomal recessive bestrophinopathy
- ORPHA:85128Bothnia retinal dystrophy
- ORPHA:209932Cone dystrophy with supernormal rod response
- ORPHA:1872Cone rod dystrophy
- ORPHA:53540Goldmann-Favre syndrome
- ORPHA:67042Late-onset retinal degeneration
- ORPHA:65Leber congenital amaurosis
- ORPHA:247834Occult macular dystrophy
- ORPHA:1871Progressive cone dystrophy
- ORPHA:352718Progressive retinal dystrophy due to retinol transport defect
- ORPHA:397758Retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies
- ORPHA:791Retinitis pigmentosa
- ORPHA:52427Retinitis punctata albescens
- ORPHA:364055Severe early-childhood-onset retinal dystrophy
- ORPHA:827Stargardt disease
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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/717324
- This record as JSON: /data/d/717324.json