ORPHA:2267
OBSOLETE: Ichthyosis-cheek-eyebrow syndrome
inactive · referred to ORPHA:281244Autosomal ichthyosis syndrome with other associated signs
Synonyms: OBSOLETE: Sidransky-Feinstein-Goodman syndrome
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Autosomal ichthyosis syndrome with other associated signs
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Ichthyosis-cheek-eyebrow syndrome | OBSOLETE: Sidransky-Feinstein-Goodman syndrome |
| fr | OBSOLETE : Syndrome d'ichtyose-joues proéminentes-sourcils latéraux | OBSOLETE : Syndrome de Sidransky-Feinstein-Goodman |
| de | OBSOLET: Ichthyose-Wangen-Augenbrauen-Syndrom | OBSOLET: Sidransky-Feinstein-Goodman-Syndrom |
| es | OBSOLETO: Síndrome de ictiosis-mejillas-cejas | OBSOLETO: Síndrome de Sidransky-Feinstein-Goodman |
| it | OBSOLETO: Sindrome ittiosi-guance-sopracciglia | OBSOLETO: Sindrome di Sidransky-Feinstein-Goodman |
| nl | OBSOLEET: Ichthyosis - wang - wenkbrauw-syndroom | OBSOLEET: Syndroom van Sidransky-Feinstein-Goodman |
| pt | OBSOLETO: Síndrome ictiose-bochecha-sobrancelha | OBSOLETO: Síndrome ICE · OBSOLETO: Síndrome Sidransky-Feinstein-Goodman |
| pl | NIEAKTUALNE: Zespól rybiej luski, policzków i brwi | NIEAKTUALNE: Zespół Sidransky'ego, Feinsteina i Goodmana |
| cs | NEAKTUÁLNÍ: Syndrom ichtyóza-tváře-obočí | NEAKTUÁLNÍ: Sidranského-Feinsteinův-Goodmanův syndrom · NEAKTUÁLNÍ: Sidranski-Feinstein-Goodmanův syndrom |
| uk | ЗАСТАРІЛО: Синдром іхтіоз-щоки-брови | ЗАСТАРІЛО: Синдром Сідранського-Фейнштейна-Гудмана |
| zh | 弃用：鱼鳞病-面颊-眉毛综合征 | Sidransky-Feinstein-Goodman 综合征 |
| tr | Eski adı: İktiyoz-yanak-kaş sendromu | Sidransky-Feinstein-Goodman 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/2267
- This record as JSON: /data/d/2267.json