ORPHA:3067
OBSOLETE: Intellectual disability-microcephaly-phalangeal-facial abnormalities syndrome
inactive · referred to ORPHA:102283Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
- 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: Intellectual disability-microcephaly-phalangeal-facial abnormalities syndrome | |
| fr | OBSOLETE : Syndrome de déficience intellectuelle-microcéphalie-anomalies phalangiennes et faciales | |
| de | OBSOLET: Intelligenzminderung mit Mikrozephalie und Anomalien des Gesichtes und der Phalangen | |
| es | OBSOLETO: Síndrome de discapacidad intelectual-microcefalia-anomalías falángicas y faciales | |
| it | OBSOLETO: Ritardo mentale - microcefalia - anomalie facciali e delle falangi | |
| nl | OBSOLEET: Intellectuele achterstand - microcefalie - falangeale en faciale afwijkingen-syndroom | |
| pt | OBSOLETO: Síndrome de perturbação do desenvolvimento intelectual-microcefalia-anomalias falângicas e faciais | |
| pl | NIEAKTUALNE: Niepelnosprawnosc intelektualna - mikrocefalia - nieprawidlowosci paliczkowo-twarzowe | |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující mentální retardaci, mikrocefalii a falangeální a faciální abnormality | |
| uk | Синдром інтелектуальної недостатності-мікроцефалії-фалангово-лицьових аномалій | |
| zh | 弃用：智力障碍-小头-指（趾）-面部畸形综合征 | |
| tr | Eski adı: zihinsel yetersizlik-mikrosefali-falangeal-yüz anormallikleri 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/3067
- This record as JSON: /data/d/3067.json