ORPHA:2099
OBSOLETE: Grix-Blankenship-Peterson syndrome
inactive · referred to ORPHA:102283Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
Synonyms: OBSOLETE: Craniofacial and osseous defects-intellectual disability 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 Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Grix-Blankenship-Peterson syndrome | OBSOLETE: Craniofacial and osseous defects-intellectual disability syndrome |
| fr | OBSOLETE : Syndrome de Grix-Blankenship-Peterson | OBSOLETE : Syndrome d'anomalies craniofaciales et osseuses-déficience intellectuelle |
| de | OBSOLET: Gris-Blankenship-Peterson-Syndrom | |
| es | OBSOLETO: Síndrome de Grix-Blankenship-Peterson | OBSOLETO: Síndrome de anomalías craneofaciales y óseas-discapacidad intelectual |
| it | OBSOLETO: Sindrome di Grix-Blankenship-Peterson | OBSOLETO: Sindrome anomalie craniofacciali e scheletriche-disabilità intellettiva |
| nl | OBSOLEET: Syndroom van Grix-Blankenship-Peterson | OBSOLEET: Craniofaciale en ossale defecten - intellectuele achterstand-syndroom |
| pt | OBSOLETO: Síndrome Grix-Blankenship-Peterson | OBSOLETO: Síndrome de anomalias craniofaciais e ósseas-perturbação do desenvolvimento intelectual |
| pl | NIEAKTUALNE: Zespól Grixa, Blankenshipa i Petersona | NIEAKTUALNE: Wady czaszkowo-twarzowe i kości - niepełnosprawność intelektualna |
| cs | NEAKTUÁLNÍ: Grixův-Blankenshipův-Petersonův syndrom | NEAKTUÁLNÍ: Syndrom zahrnující kraniofaciální a kostní defekty a mentální retardaci |
| uk | Синдром Грікса-Бланкеншипа-Пітерсона | ЗАСТАРІЛО: Синдром черепно-лицьових та кісткових дефектів - інтелектуальної недостатності |
| zh | 弃用：Grix-Blankenship-Peterson综合征 | 颅面和骨缺陷-智力障碍综合征 |
| tr | Eski adı: Grix-Blankenship-Peterson sendromu | Kraniyofasiyal ve kemik defektleri-zihinsel yetersizlik 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/2099
- This record as JSON: /data/d/2099.json