{"orpha":3357,"name":"OBSOLETE: Autosomal dominant trichoodontoonychodysplasia-syndactyly","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Trueb-Burg-Bottani syndrome"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Ectodermal dysplasia syndrome","url":"https://raremap.alftech.space/d/ORPHA-3357/","orphanet_url":"https://www.orpha.net/en/disease/detail/3357","names":{"fr":{"name":"OBSOLETE : Syndrome de dysplasie tricho-odonto-onychiale-syndactylie autosomique dominante","synonyms":["OBSOLETE : Syndrome de Trueb-Burg-Bottani"]},"de":{"name":"OBSOLET: Tricho-odonto-onycho-Dysplasie mit Syndaktylie","synonyms":["OBSOLET: Trueb-Burg-Bottani-Syndrom"]},"es":{"name":"OBSOLETO: Displasia trico-odonto-oniquial-sindactilia autosómica dominante","synonyms":["OBSOLETO: Síndrome de Trueb-Burg-Bottani"]},"it":{"name":"OBSOLETO: Trico-dento-onico-displasia-sindattilia, autosomica dominante","synonyms":["OBSOLETO: Sindrome di Trueb-Burg-Bottani"]},"nl":{"name":"OBSOLEET: Autosomaal dominante tricho-odonto-onychodysplasie - syndactylie","synonyms":["OBSOLEET: Syndroom van Trueb-Burg-Bottani"]},"pt":{"name":"OBSOLETO: Displasia trico-odonto-ungueal-sindactilia autossómica dominante"},"pl":{"name":"NIEAKTUALNE: Dysplazja wlosowo-zebowo-paznokciowa - syndaktylia dominujaca","synonyms":["NIEAKTUALNE: Zespół Trueba, Burga i Bottaniego"]},"cs":{"name":"NEAKTUÁLNÍ: Autozomálně dominantní trichoodontoonychodysplázie a syndaktylie","synonyms":["NEAKTUÁLNÍ: Truebův-Burgův-Bottaniho syndrom","NEAKTUÁLNÍ: Trueb-Burg-Bottaniho syndrom"]},"uk":{"name":"ЗАСТАРІЛО: Аутосомно-домінантна трихоодонтооніходисплазія-синдактилія","synonyms":["ЗАСТАРІЛО: Синдром Труба-Бург-Боттані"]},"zh":{"name":"弃用：常染色体显性遗传毛发牙齿甲床发育不良-并指(趾)","synonyms":["Trueb-Burg-Bottani综合征"]},"tr":{"name":"Eski adı: Otozomal dominant trikoodontoonikodisplazi-sindaktili","synonyms":["Trueb-Burg-Bottani sendromu"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":79373,"name":"Ectodermal dysplasia syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}