raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
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
LangNameSynonyms
enOBSOLETE: Autosomal dominant trichoodontoonychodysplasia-syndactylyOBSOLETE: Trueb-Burg-Bottani syndrome
frOBSOLETE : Syndrome de dysplasie tricho-odonto-onychiale-syndactylie autosomique dominanteOBSOLETE : Syndrome de Trueb-Burg-Bottani
deOBSOLET: Tricho-odonto-onycho-Dysplasie mit SyndaktylieOBSOLET: Trueb-Burg-Bottani-Syndrom
esOBSOLETO: Displasia trico-odonto-oniquial-sindactilia autosómica dominanteOBSOLETO: Síndrome de Trueb-Burg-Bottani
itOBSOLETO: Trico-dento-onico-displasia-sindattilia, autosomica dominanteOBSOLETO: Sindrome di Trueb-Burg-Bottani
nlOBSOLEET: Autosomaal dominante tricho-odonto-onychodysplasie - syndactylieOBSOLEET: Syndroom van Trueb-Burg-Bottani
ptOBSOLETO: Displasia trico-odonto-ungueal-sindactilia autossómica dominante
plNIEAKTUALNE: Dysplazja wlosowo-zebowo-paznokciowa - syndaktylia dominujacaNIEAKTUALNE: Zespół Trueba, Burga i Bottaniego
csNEAKTUÁLNÍ: Autozomálně dominantní trichoodontoonychodysplázie a syndaktylieNEAKTUÁLNÍ: Truebův-Burgův-Bottaniho syndrom · NEAKTUÁLNÍ: Trueb-Burg-Bottaniho syndrom
ukЗАСТАРІЛО: Аутосомно-домінантна трихоодонтооніходисплазія-синдактиліяЗАСТАРІЛО: 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
trEski adı: Otozomal dominant trikoodontoonikodisplazi-sindaktiliTrueb-Burg-Bottani sendromu
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Cross-references

qualifier = Orphanet mapping relation

No cross-references in this release.

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Classification

Not placed in any Orphanet classification in this release.

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

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Prevalence and incidence

0 records

No prevalence record in this release.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

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Sources for this card