ORPHA:3360
OBSOLETE: Trichodermal syndrome-intellectual disability syndrome
inactive · referred to ORPHA:102369Rare syndromic intellectual disability
Synonyms: OBSOLETE: Katsantoni-Papadakou Lagoyanni 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: Trichodermal syndrome-intellectual disability syndrome | OBSOLETE: Katsantoni-Papadakou Lagoyanni syndrome |
| fr | OBSOLETE : Syndrome trichodermal-déficience intellectuelle | OBSOLETE : Syndrome de Katsantoni-Papadakou-Lagoyanni |
| de | OBSOLET: Trichodermales Syndrom-Intelligenzminderung-Syndrom | OBSOLET: Katsantoni-Papadakou-Lagoyanni-Syndrom |
| es | OBSOLETO: Síndrome tricodérmico-discapacidad intelectual | OBSOLETO: Síndrome de Katsantoni-Papadakou Lagoyanni |
| it | OBSOLETO: Sindrome tricodermica-disabilità intellettiva | OBSOLETO: Sindrome di Katsantoni-Papadakou-Lagoyanni |
| nl | OBSOLEET: Trichodermaal syndroom - intellectuele achterstand-syndroom | OBSOLEET: Syndroom van Katsantoni-Papadakou Lagoyanni |
| pt | OBSOLETO: Síndrome tricodérmico-perturbação do desenvolvimento intelectual | OBSOLETO: Síndrome Katsantoni-Papadakou-Lagoyanni |
| pl | NIEAKTUALNE: Zespól wlosowo - skórny - niepelnosprawnosc intelektualna | NIEAKTUALNE: Zespół Katsantoni, Papadakou i Lagoyanni |
| cs | NEAKTUÁLNÍ: Syndrom zahrnující trichodermální syndrom a mentální retardaci | NEAKTUÁLNÍ: Katsantoniové-Papadakou Lagoyanniho syndrom · NEAKTUÁLNÍ: Katsantoni-Papadakou Lagoyanniho syndrom |
| uk | ЗАСТАРІЛО: Триходермальний синдром - синдром інтелектуальної недостатності | ЗАСТАРІЛО: Синдром Катсантоні-Пападаку-Лагоянні |
| zh | 弃用：木霉属综合征-智力障碍综合征 | Katsantoni-Papadakou Lagoyanni综合征 |
| tr | Eski adı: Trikodermal sendrom-zihinsel yetersizlik sendromu | Katsantoni-Papadakou Lagoyanni 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/3360
- This record as JSON: /data/d/3360.json