ORPHA:3046
OBSOLETE: Intellectual disability-unusual facies, Davis-Lafer type
inactive · referred to ORPHA:102369Rare syndromic intellectual disability
Synonyms: OBSOLETE: Davis-Lafer 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 Rare syndromic intellectual disability
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Intellectual disability-unusual facies, Davis-Lafer type | OBSOLETE: Davis-Lafer syndrome |
| fr | OBSOLETE : Syndrome de déficience intellectuelle-facis anormal, type Davis-Lafer | OBSOLETE : Syndrome de Davis-Lafer |
| de | OBSOLET: Intelligenzminderung mit Gesichtsanomalien Typ Davis-Lafer | OBSOLET: Davis-Lafer-Syndrom |
| es | OBSOLETO: Discapacidad intelectual-facies inusual tipo Davis-Lafer | OBSOLETO: Síndrome de Davis-Lafer |
| it | OBSOLETO: Disabilità intellettiva-anomalie facciali, tipo Davis Lafer | OBSOLETO: Sindrome di Davis-Lafer |
| nl | OBSOLEET: Intellectuele achterstand - ongewoon uiterlijk, Davis-Lafer-type | OBSOLEET: Davis-Lafersyndroom |
| pt | OBSOLETO: Perturbação do desenvolvimento intelectual-face peculiar, tipo Davis-Lafer | OBSOLETO: Síndrome Davis-Lafer |
| pl | NIEAKTUALNE: Niepelnosprawnosc intelektualna - niezwykla twarz typu Davisa i Lafera | NIEAKTUALNE: Zespół Davisa i Lafera |
| cs | NEAKTUÁLNÍ: Mentální retardaci a neobvyklá tvář, typ Davis-Lafer | = en |
| uk | ЗАСТАРІЛО: Розумова відсталість - незвичайні риси обличчя, тип Девіса-Лафера | ЗАСТАРІЛО: Синдром Девіса-Лафера |
| zh | 弃用：智力障碍-异常面容综合征， Davis-Lafer亚型 | Davis-Lafer综合征 |
| tr | Eski adı: Zihinsel yetersizlik-alışılmadık yüz, Davis-Lafer tipi | Davis-Lafer 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/3046
- This record as JSON: /data/d/3046.json