{"orpha":453,"name":"IBIDS syndrome","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":["Tay syndrome","Trichothiodystrophy type E","Trichothiodystrophy with congenital ichthyosis"],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Trichothiodystrophy","url":"https://raremap.alftech.space/d/ORPHA-453/","orphanet_url":"https://www.orpha.net/en/disease/detail/453","names":{"fr":{"name":"Syndrome IBIDS","synonyms":["Ichtyose avec trichothiodystrophie","Syndrome de Tay","Trichothiodystrophie type E"]},"de":{"name":"IBIDS-Syndrom","synonyms":["Tay-Syndrom","Trichothiodystrophie Typ E","Trichothiodystrophie mit kongenitaler Ichthyose"]},"es":{"name":"Síndrome IBIDS"},"it":{"name":"Sindrome IBIDS","synonyms":["Sindrome di Tay","Tricotiodistrofia con ittiosi congenita","Tricotiodistrofia, tipo E"]},"nl":{"name":"IBIDS-syndroom","synonyms":["Taysyndroom","Trichothiodystrofie met congenitale ichthyosis","Trichothiodystrofie type E"]},"pt":{"name":"Síndrome IBIDS","synonyms":["Síndrome Tay","Tricotiodistrofia tipo E","Tricotiodistrofia-ictiose congénita"]},"pl":{"name":"Zespół IBIDS","synonyms":["Trichotiodystrofia typu E","Trichotiodystrofia z rybią łuską wrodzoną","Zespół Tay'a"]},"cs":{"name":"IBIDS syndrom","synonyms":["Trichothiodystrofie, typ E","Trichothiodystrofie s vrozenou ichtyózou","Tayův syndrom"]},"uk":{"name":"Синдром IBIDS","synonyms":["Синдром Тея","Трихотіодистрофія типу Е","Трихотіодистрофія з вродженим іхтіозом"]},"zh":{"name":"IBIDS综合征","synonyms":["毛发低硫营养不良伴先天性鱼鳞病"]},"tr":{"name":"IBIDS sendromu","synonyms":["Tay sendromu","Trikotiyodistrofi tip E","Doğumsal iktiyozlu trikotiyodistrofi"]}},"xrefs":[{"source":"UMLS","code":"C1866505","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":33364,"name":"Trichothiodystrophy"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}