ORPHA:3357
OBSOLETE: Autosomal dominant trichoodontoonychodysplasia-syndactyly
inactive · referred to ORPHA:79373Ectodermal dysplasia syndrome
Synonyms: OBSOLETE: Trueb-Burg-Bottani 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 Ectodermal dysplasia syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Autosomal dominant trichoodontoonychodysplasia-syndactyly | OBSOLETE: Trueb-Burg-Bottani syndrome |
| fr | OBSOLETE : Syndrome de dysplasie tricho-odonto-onychiale-syndactylie autosomique dominante | OBSOLETE : Syndrome de Trueb-Burg-Bottani |
| de | OBSOLET: Tricho-odonto-onycho-Dysplasie mit Syndaktylie | OBSOLET: Trueb-Burg-Bottani-Syndrom |
| es | OBSOLETO: Displasia trico-odonto-oniquial-sindactilia autosómica dominante | OBSOLETO: Síndrome de Trueb-Burg-Bottani |
| it | OBSOLETO: Trico-dento-onico-displasia-sindattilia, autosomica dominante | OBSOLETO: Sindrome di Trueb-Burg-Bottani |
| nl | OBSOLEET: Autosomaal dominante tricho-odonto-onychodysplasie - syndactylie | OBSOLEET: Syndroom van Trueb-Burg-Bottani |
| pt | OBSOLETO: Displasia trico-odonto-ungueal-sindactilia autossómica dominante | |
| pl | NIEAKTUALNE: Dysplazja wlosowo-zebowo-paznokciowa - syndaktylia dominujaca | NIEAKTUALNE: Zespół Trueba, Burga i Bottaniego |
| cs | NEAKTUÁLNÍ: Autozomálně dominantní trichoodontoonychodysplázie a syndaktylie | NEAKTUÁLNÍ: Truebův-Burgův-Bottaniho syndrom · NEAKTUÁLNÍ: Trueb-Burg-Bottaniho syndrom |
| uk | ЗАСТАРІЛО: Аутосомно-домінантна трихоодонтооніходисплазія-синдактилія | ЗАСТАРІЛО: Синдром Труба-Бург-Боттані |
| zh | 弃用:常染色体显性遗传毛发牙齿甲床发育不良-并指(趾) | Trueb-Burg-Bottani综合征 |
| tr | Eski adı: Otozomal dominant trikoodontoonikodisplazi-sindaktili | Trueb-Burg-Bottani 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/3357
- This record as JSON: /data/d/3357.json