ORPHA:98696
OBSOLETE: Genodermatosis with ocular features
inactive · referred to ORPHA:68346Rare genetic skin disease
- 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 skin disease
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Genodermatosis with ocular features | |
| fr | OBSOLETE : Génodermatose avec atteintes oculaires | |
| de | OBSOLET: Genodermatose mit Augenbeteiligung | |
| es | OBSOLETO: Genodermatosis con manifestaciones oculares | |
| it | OBSOLETO: Genodermatosi con segni oculari | |
| nl | OBSOLEET: Genodermatose met oculaire kenmerken | |
| pt | OBSOLETO: Genodermatose com doença ocular | |
| pl | NIEAKTUALNE: Genodermatoza z objawami ocznymi | |
| cs | NEAKTUÁLNÍ: Genodermatózy s očními příznaky | |
| uk | ЗАСТАРІЛО: Генодерматоз з очними ознаками | |
| zh | 弃用：遗传性皮肤病伴眼特征 | |
| tr | Eski adı: Oküler özellikler ile seyreden genodermatoz |
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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/98696
- This record as JSON: /data/d/98696.json