ORPHA:183598
OBSOLETE: Rare genetic palpebral, lacrimal system and conjunctival disease
inactive · referred to ORPHA:522524Rare genetic disorder of the ocular adnexa
- 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 disorder of the ocular adnexa
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Rare genetic palpebral, lacrimal system and conjunctival disease | |
| fr | OBSOLETE : Maladie génétique de la paupière, de l'appareil lacrymal et de la conjonctive | |
| de | OBSOLET: Seltene Krankheiten des palpebralen, lakrimalen und konjunktivalen Systems, genetisch bedingt | |
| es | OBSOLETO: Enfermedad genética rara de los párpados, del sistema lagrimal y de la conjuntiva | |
| it | OBSOLETO: Malattia genetica rara della palpebra, dell'apparato lacrimale e della congiuntiva | |
| nl | OBSOLEET: Zeldzame genetische palpebrale, traansysteem- en conjunctivale ziektes | |
| pt | OBSOLETO: Doença palpebral, do sistema lacrimal e conjuntiva, genética rara | |
| pl | NIEAKTUALNE: Rzadka genetyczna choroba powiek, ukladu lzowego i spojówek | |
| cs | NEAKTUÁLNÍ: Vzácná geneticky podmíněná onemocnění víček, spojivky a slzných kanálků | |
| uk | ЗАСТАРІЛО: Рідкісне генетично обумовлене захворювання повік, слізної системи та конюнктиви | |
| zh | 弃用：罕见遗传性睑、泪腺和结膜疾病 | |
| tr | Eski adı: Nadir genetik palpebral, lakrimal sistem ve konjonktival hastalık |
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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/183598
- This record as JSON: /data/d/183598.json