ORPHA:217046
OBSOLETE: Autosomal recessive childhood-onset cortical cataract
inactive · referred to ORPHA:98992Early-onset partial cataract
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Early-onset partial cataract
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Autosomal recessive childhood-onset cortical cataract | |
| fr | OBSOLETE : Cataracte corticale de l'enfant autosomique récessive | |
| de | OBSOLET: Kortikale Katarakt des Kindesalters, autosomal-rezessiv | OBSOLET: Cataracta corticalis · OBSOLET: Rindenkatarakt, pädiatrische |
| es | OBSOLETO: Catarata cortical autosómica recesiva de inicio en la infancia | |
| it | OBSOLETO: Cataratta corticale autosomica recessiva a esordio nell'infanzia | |
| nl | OBSOLEET: Autosomaal recessief corticaal cataract met aanvang in de kindertijd | |
| pt | OBSOLETO: Catarata cortical autossómica recessiva de início na infância | |
| pl | NIEAKTUALNE: Autosomalna recesywna zacma korowa o poczatku w wieku dzieciecym | |
| cs | NEAKTUÁLNÍ: Autozomálně recesivní kortikální katarakta v dětství | |
| uk | ЗАСТАРІЛО: Аутосомно-рецесивна дитяча кортикальна катаракта | |
| zh | 弃用:常染色体隐性遗传儿童期起病的皮质性白内障 | |
| tr | Eski adı: Otozomal resesif çocukluk başlangıçlı kortikal katarakt |
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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/217046
- This record as JSON: /data/d/217046.json