ORPHA:1562
OBSOLETE: Dacryocystitis-osteopoikilosis syndrome
inactive · referred to ORPHA:93444Primary bone dysplasia with increased bone density
Synonyms: OBSOLETE: Gunal-Seber-Basaran syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Primary bone dysplasia with increased bone density
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Dacryocystitis-osteopoikilosis syndrome | OBSOLETE: Gunal-Seber-Basaran syndrome |
| fr | OBSOLETE : Syndrome de dacryocystite-ostéopoecilie | OBSOLETE : Syndrome de Gunal-Seber-Basaran · OBSOLETE : Syndrome de dacryocystite-ostéopoïkilose |
| de | OBSOLET: Dakryozystitis-Osteopoikilose-Syndrom | OBSOLET: Gunal-Seber-Basaran-Syndrom |
| es | OBSOLETO: Síndrome de dacriocistitis-osteopoiquilosis | OBSOLETO: Síndrome de Gunal-Seber-Basaran |
| it | OBSOLETO: Sindrome dacriocistite-osteopoichilosi | OBSOLETO: Sindrome di Gunal-Seber-Basaran |
| nl | OBSOLEET: Dacryocystitis - osteopoikilose-syndroom | OBSOLEET: Syndroom van Gunal-Seber-Basaran |
| pt | OBSOLETO: Síndrome de dacriocistite-osteopoiquilose | OBSOLETO: Síndrome Gunal-Seber-Basaran |
| pl | NIEAKTUALNE: Zespół zapalenia woreczka łzowego - osteopoikilozy | NIEAKTUALNE: Zespół Gunala, Sebera i Basarana |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující dakryocystitidu a osteopoikilózu | NEAKTUÁLNÍ: Gunalův-Seberův-Basaranův syndrom · NEAKTUÁLNÍ: Gunal-Seber-Basaranův syndrom |
| uk | ЗАСТАРІЛО: Синдром дакріоциститу-остеопойкілозу | ЗАСТАРІЛО: Синдром Гунал-Себера-Басарана |
| zh | 泪囊炎-骨斑点病综合征 | Gunal-Seber-Basaran综合征 |
| tr | Dakriyosistit-osteopoikiloz sendromu | Günal-Seber-Başaran sendromu |
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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/1562
- This record as JSON: /data/d/1562.json