{"orpha":1651,"name":"OBSOLETE: Dennis-Cohen syndrome","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.<br/><br/>Instead, consider using Multiple congenital anomalies/dysmorphic syndrome-intellectual disability","url":"https://raremap.alftech.space/d/ORPHA-1651/","orphanet_url":"https://www.orpha.net/en/disease/detail/1651","names":{"fr":{"name":"OBSOLETE : Syndrome de Dennis-Cohen"},"de":{"name":"OBSOLET: Dennis-Cohen-Syndrom"},"es":{"name":"OBSOLETO: Síndrome de Dennis Cohen"},"it":{"name":"OBSOLETO: Sindrome di Dennis-Cohen"},"nl":{"name":"OBSOLEET: Syndroom van Dennis-Cohen"},"pt":{"name":"OBSOLETO: Síndrome Dennis-Cohen"},"pl":{"name":"NIEAKTUALNE: Zespól Dennisa i Cohena"},"cs":{"name":"NEAKTUÁLNÍ: Dennis-Cohenův syndrom"},"uk":{"name":"ЗАСТАРІЛО: Синдром Денніса-Коена"},"zh":{"name":"弃用：Dennis-Cohen综合征"},"tr":{"name":"Eski adı: Dennis-Cohen sendromu"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":102283,"name":"Multiple congenital anomalies/dysmorphic syndrome-intellectual disability"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}