{"orpha":163953,"name":"X-linked intellectual disability, Raymond type","type":"Disease","group":"Disorder","status":"inactive","flags":["Deprecated entity"],"synonyms":[],"definition":null,"note":"This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Lujan-Fryns syndrome","url":"https://raremap.alftech.space/d/ORPHA-163953/","orphanet_url":"https://www.orpha.net/en/disease/detail/163953","names":{"fr":{"name":"Déficience intellectuelle liée à l'X type Raymond"},"de":{"name":"Intelligenzminderung, X-chromosomale, Typ Raymond"},"es":{"name":"Discapacidad intelectual ligada al cromosoma X tipo Raymond"},"it":{"name":"Disabilità intellettiva legata all'X, tipo Raymond"},"nl":{"name":"X-gebonden intellectuele achterstand, Raymond-type"},"pt":{"name":"Perturbação do desenvolvimento intelectual ligada ao X, tipo Raymond"},"pl":{"name":"Niepełnosprawność intelektualna sprzężona z chromosomem X, typ Raymonda"},"cs":{"name":"X-vázaná mentální retardace, Raymondové typ"},"uk":{"name":"Х-зчеплена розумова відсталість, тип Реймонда"},"zh":{"name":"Raymond 型X连锁型智力障碍综合征"},"tr":{"name":"X'e bağlı zihinsel yetersizlik, Raymond tipi"}},"xrefs":[{"source":"OMIM","code":"300799","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":776,"name":"Lujan-Fryns syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}