ORPHA:717336
Rare genetic isolated progressive predominantly macular disorder
- 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 predominantly macular disorder | |
| fr | Maladie génétique rare isolée avec atteinte progressive prédominante de la macula | |
| de | Seltene genetische isolierte progrediente Makulopathie | |
| es | Trastorno genético raro predominantemente macular progresivo aislado | |
| it | Malattia genetica rara progressiva a predominanza maculare isolata | |
| nl | Zeldzame genetische geïsoleerde progressieve aandoening van voornamelijk macula | Zeldzame genetische geïsoleerde progressieve aandoening van voornamelijk gele vlek · Zeldzame genetische geïsoleerde progressieve overwegend maculaire aandoening |
| pt | Rare genetic isolated progressive predominantly macular disorder | |
| pl | Rzadkie genetycznie uwarunkowane izolowane postępujące zaburzenie dotyczące głównie plamki | |
| cs | Rare genetic isolated progressive predominantly macular disorder |
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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:717333Rare genetic progressive predominantly macular disorder
rare genetic diseases
Children (15):
- ORPHA:75376Autosomal dominant drusen
- ORPHA:139455Autosomal recessive bestrophinopathy
- ORPHA:1243Best vitelliform macular dystrophy
- ORPHA:41751Bietti crystalline dystrophy
- ORPHA:75377Central areolar choroidal dystrophy
- ORPHA:75381Cystoid macular dystrophy
- ORPHA:67042Late-onset retinal degeneration
- ORPHA:263347MRCS syndrome
- ORPHA:466718Martinique crinkled retinal pigment epitheliopathy
- ORPHA:247834Occult macular dystrophy
- ORPHA:63454Pattern dystrophy
- ORPHA:319640Retinal macular dystrophy type 2
- ORPHA:59181Sorsby fundus dystrophy
- ORPHA:827Stargardt disease
- ORPHA:792X-linked retinoschisis
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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/717336
- This record as JSON: /data/d/717336.json