ORPHA:1060
Systemic cystic angiomatosis-Seip syndrome
inactive · moved to ORPHA:528Congenital generalized lipodystrophy
Synonyms: Brunzell syndrome
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Congenital generalized lipodystrophy
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Systemic cystic angiomatosis-Seip syndrome | Brunzell syndrome |
| fr | Syndrome d'angiomatose kystique-syndrome de Seip | Syndrome de Brunzell |
| de | Systemische zystische Angiomatose-Seip-Syndrom | Brunzell-Syndrom |
| es | Angiomatosis quística sistémica-síndrome de Seip | Síndrome de Brunzell |
| it | Angiomatosi cistica - sindrome di Seip | |
| nl | Systemische cystische angiomatose - syndroom van Seip | Syndroom van Brunzell |
| pt | Síndrome Seip-angiomatose quística sistémica | |
| pl | Zespół Seipa | Zespół Brunzella |
| cs | Systémová cystická angiomatóza a Seipův syndrom | Brunzellův syndrom |
| uk | Системний кістозний ангіоматоз - синдром Сейпа | Синдром Брунзеля |
| zh | 系统性囊状血管瘤-赛普综合征 | Brunzell综合征 |
| tr | Sistemik kistik anjiyomatoz-Seip sendromu | Brunzell 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/1060
- This record as JSON: /data/d/1060.json