ORPHA:98700
OBSOLETE: Pigmentation disorder with eye involvement
inactive · referred to ORPHA:79374Pigmentation anomaly of the skin
- 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 Pigmentation anomaly of the skin
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Pigmentation disorder with eye involvement | |
| fr | OBSOLETE : Anomalie de la pigmentation cutanée avec atteinte ophtalmologique | |
| de | OBSOLET: Pigmentierungsstörung mit assoziierter Augenbeteiligung | |
| es | OBSOLETO: Trastorno de la pigmentación con afectación ocular | |
| it | OBSOLETO: Disturbo della pigmentazione associato a malattia oculare | |
| nl | OBSOLEET: Pigmentatiestoornis met betrokkenheid van oog | |
| pt | OBSOLETO: Doença ocular associada a alteração da pigmentação | |
| pl | NIEAKTUALNE: Zaburzenia barwnikowe z objawami ocznymi | |
| cs | NEAKTUÁLNÍ: Poruchy pigmentace s postižením očí | |
| uk | ЗАСТАРІЛО: Порушення пігментації з ураженням очей | |
| zh | 弃用：色素沉着障碍伴眼受累 | |
| tr | Eski adı: Göz tutulumu ile seyreden pigmentasyon bozukluğu |
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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/98700
- This record as JSON: /data/d/98700.json