ORPHA:3043
OBSOLETE: Intellectual disability-unusual facies syndrome
inactive · referred to ORPHA:102369Rare syndromic intellectual disability
Synonyms: OBSOLETE: Morillo Cucci-Passarge 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 syndrome | OBSOLETE: Morillo Cucci-Passarge syndrome |
| fr | OBSOLETE : Syndrome de déficience intellectuelle-dysmorphie-hyperlaxité | OBSOLETE : Syndrome de Morillo-Cucci-Passarge |
| de | OBSOLET: Intelligenzminderung-ungewöhnliche Fazies-Syndrom | OBSOLET: Morillo-Cucci-Passarge-Syndrom |
| es | OBSOLETO: Síndrome de discapacidad intelectual-facies inusual | OBSOLETO: Síndrome de Morillo Cucci-Passarge |
| it | OBSOLETO: Sindrome disabilità intellettiva-dismorfismi | OBSOLETO: Sindrome di Morillo-Cucci-Passarge |
| nl | OBSOLEET: Intellectuele achterstand - ongewoon uiterlijk-syndroom | OBSOLEET: Syndroom van Morillo Cucci-Passarge |
| pt | OBSOLETO: Síndrome de perturbação do desenvolvimento intelectual-face peculiar | OBSOLETO: Síndrome Morillo-Cucci-Passarge |
| pl | NIEAKTUALNE: Niepelnosprawnosc intelektualna - niezwykla twarz | NIEAKTUALNE: Zespół Morillo Cucci i Passarge |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující mentální retardaci a neobvyklou tvář | = en |
| uk | ЗАСТАРІЛО: Синдром розумової відсталості з незвичайними рисами обличчям | ЗАСТАРІЛО: Синдром Морілло-Куччі-Пассаржа: синдром Морілло-Куччі-Пассаржа |
| zh | 弃用：智力障碍-异常面容综合征 | Morillo Cucci-Passarge综合征 |
| tr | Eski adı: zihinsel yetersizlik-alışılmadık yüz sendromu | Morillo Cucci-Passarge 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/3043
- This record as JSON: /data/d/3043.json