{"orpha":3417,"name":"OBSOLETE: Van den Bosch syndrome","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"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-3417/","orphanet_url":"https://www.orpha.net/en/disease/detail/3417","names":{"fr":{"name":"OBSOLETE : Syndrome de Van der Bosch"},"de":{"name":"OBSOLET: Van den Bosch-Syndrom"},"es":{"name":"OBSOLETO: Síndrome de Van der Bosch"},"it":{"name":"OBSOLETO: Sindrome Van den Bosch"},"nl":{"name":"OBSOLEET: Syndroom van Van den Bosch"},"pt":{"name":"OBSOLETO: Síndrome Van den Bosch"},"pl":{"name":"NIEAKTUALNE: Zespół van den Boscha"},"cs":{"name":"NEAKTUÁLNÍ: Van den Boschův syndrom"},"uk":{"name":"Синдром Ван ден Боша","definition":"A rare X-linked syndromic intellectual disability characterized by intellectual deficit, choroideremia, horizontal nystagmus, severe myopia, acrokeratosis verruciformis-like skin abnormality, anhidrosis, and scapular winging. There have been no further descriptions in the literature since 1959."},"zh":{"name":"Van den Bosch综合征"},"tr":{"name":"Van den Bosch 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}