ORPHA:3313
OBSOLETE: Intellectual disability-microcephaly-unusual facies syndrome
inactive · referred to ORPHA:102283Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
Synonyms: OBSOLETE: Thiele 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 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-unusual facies syndrome | OBSOLETE: Thiele syndrome |
| fr | OBSOLETE : Syndrome de Theile | OBSOLETE : Déficience intellectuelle-microcéphalie-faciès particulier |
| de | OBSOLET: Intelligenzminderung-Mikrozephalie-ungewöhnliche Fazies-Syndrom | OBSOLET: Thiele-Syndrom |
| es | OBSOLETO: Síndrome de discapacidad intelectual-microcefalia-facies inusual | OBSOLETO: Síndrome de Thiele |
| it | OBSOLETO: Sindrome disabilità intellettiva-microcefalia-facies caratteristica | OBSOLETO: Sindrome di Thiele |
| nl | OBSOLEET: Intellectuele achterstand - microcefalie - ongewoon gelaat-syndroom | OBSOLEET: Syndroom van Thiele |
| pt | OBSOLETO: Síndrome de perturbação do desenvolvimento intelectual-microcefalia-face peculiar | OBSOLETO: Síndrome Thiele |
| pl | NIEAKTUALNE: Niepelnosprawnosc intelektualna - maloglowie - niezwykly wyglad twarzy | NIEAKTUALNE: Zespół Thiele |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující mentální retardaci, mikrocefalii a neobvyklé facie | = en |
| uk | ЗАСТАРІЛО: Синдром розумової відсталості-мікроцефалії-незвичайної зовнішності | ЗАСТАРІЛО: Синдром Тіле |
| zh | 弃用:智力障碍-小头畸形-特殊面容综合征 | Thiele综合征 |
| tr | Eski adı: zihinsel yetersizlik-mikrosefali-alışılmadık yüz sendromu | Thiele 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/3313
- This record as JSON: /data/d/3313.json