ORPHA:98666
OBSOLETE: Unclassified primitive or secondary maculopathy
inactive · referred to ORPHA:522572Rare genetic retinal disorder
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Rare genetic retinal disorder
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Unclassified primitive or secondary maculopathy | |
| fr | OBSOLETE : Maculopathie primaire ou secondaire non classifiée | |
| de | OBSOLET: Makulopathie, primäre oder sekundäre, sonstige | |
| es | OBSOLETO: Maculopatía primaria o secundaria no clasificada | |
| it | OBSOLETO: Maculopatia primaria o secondaria non classificata | |
| nl | OBSOLEET: Niet-geclassificeerde primitieve of secundaire maculopathie | |
| pt | OBSOLETO: Maculopatia primária ou secundária, outras | |
| pl | NIEAKTUALNE: Niesklasyfikowana makulopatia pierwotna lub wtórna | |
| cs | NEAKTUÁLNÍ: Neklasifikované primitivní nebo sekundární makulopatie | |
| uk | ЗАСТАРІЛО: некласифікована первинна або вторинна макулопатія | |
| zh | 弃用：未分类原发性或继发性黄斑病变 | |
| tr | Eski adı: Sınıflandırılmamış primitif veya sekonder makülopati |
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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/98666
- This record as JSON: /data/d/98666.json