{"orpha":3056,"name":"X-linked intellectual disability, Brooks type","type":"Malformation syndrome","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 Non-specific syndromic intellectual disability","url":"https://raremap.alftech.space/d/ORPHA-3056/","orphanet_url":"https://www.orpha.net/en/disease/detail/3056","names":{"fr":{"name":"Déficience intellectuelle liée à l'X type Brooks"},"de":{"name":"Intelligenzminderung, X-chromosomale, Typ Brooks"},"es":{"name":"Discapacidad intelectual ligada al cromosoma X tipo Brooks"},"it":{"name":"Disabilità intellettiva legata all'X, tipo Brooks"},"nl":{"name":"X-gebonden intellectuele achterstand, Brooks-type"},"pt":{"name":"Perturbação do desenvolvimento intelectual ligada ao X, tipo Brooks"},"pl":{"name":"Niepełnosprawność intelektualna sprzężona z chromosomem X typu Brooksa"},"cs":{"name":"X-vázaná mentální retardace, Brooksův typ"},"uk":{"name":"Х-зчеплена розумова відсталість, тип Брукса"},"zh":{"name":"X连锁智力障碍，Brooks亚型"},"tr":{"name":"X'e bağlı zihinsel yetersizlik, Brooks tipi"}},"xrefs":[],"associations":[{"type":"Moved to","orpha":528084,"name":"Non-specific syndromic intellectual disability"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}