{"orpha":261512,"name":"OBSOLETE: Retinitis pigmentosa and intellectual disability due to monosomy Xp11.3","type":"Malformation syndrome","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Retinitis pigmentosa and intellectual disability due to Xp11.3 microdeletion","OBSOLETE: Retinitis pigmentosa and intellectual disability due to del(X)(p11.3)"],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using X-linked intellectual disability-retinitis pigmentosa syndrome","url":"https://raremap.alftech.space/d/ORPHA-261512/","orphanet_url":"https://www.orpha.net/en/disease/detail/261512","names":{"fr":{"name":"OBSOLETE : Rétinite pigmentaire et déficience intellectuelle dues à une monosomie Xp11.3","synonyms":["OBSOLETE : Rétinite pigmentaire et déficience intellectuelle dues à une del(X)(p11.3)","OBSOLETE : Rétinite pigmentaire et déficience intellectuelle dues à une microdélétion Xp11.3"]},"de":{"name":"OBSOLET: Retinitis pigmentosa and Intelligenzminderung durch Monosomie Xp11.3","synonyms":["OBSOLET: Retinitis pigmentosa and Intelligenzminderung durch Del(X)(p11.3)","OBSOLET: Retinitis pigmentosa and Intelligenzminderung durch Mikrodeletion Xp11.3"]},"es":{"name":"OBSOLETO: Retinosis pigmentaria y discapacidad intelectual por monosomía Xp11.3","synonyms":["OBSOLETO: Retinosis pigmentaria y discapacidad intelectual por del(X)(p11.3)","OBSOLETO: Retinosis pigmentaria y discapacidad intelectual por microdeleción Xp11.3"]},"it":{"name":"OBSOLETO: Retinite pigmentosa e deficit cognitivo da monosomia Xp11.3","synonyms":["OBSOLETO: Retinite pigmentosa e deficit cognitivo da del(X)(p11.3)","OBSOLETO: Retinite pigmentosa e deficit cognitivo da microdelezione Xp11.3"]},"nl":{"name":"OBSOLEET: Retinitis pigmentosa en intellectuele achterstand door monosomie Xp11.3","synonyms":["OBSOLEET: Retinitis pigmentosa en intellectuele achterstand door Xp11.3 microdeletie","OBSOLEET: Retinitis pigmentosa en intellectuele achterstand door del(X)(p11.3)"]},"pt":{"name":"OBSOLETO: Retinite pigmentosa e perturbação do desenvolvimento intelectual por monossomia Xp11.3"},"pl":{"name":"NIEAKTUALNE: Zwyrodnienie barwnikowe siatkówki i niepelnosprawnosc intelektualna z powodu monosomii Xp11.3","synonyms":["NIEAKTUALNE: Zwyrodnienie barwnikowe siatkówki i niepełnosprawność intelektualna z powodu del(X)(p11.3)","NIEAKTUALNE: Zwyrodnienie barwnikowe siatkówki i niepełnosprawność intelektualna z powodu mikrodelecji Xp11.3"]},"cs":{"name":"NEAKTUÁLNÍ: Retinitis pigmentosa a mentální postižení způsobené monozomií Xp11.3","synonyms":["OBSOLETE: Retinitis pigmentosa and intellectual disability due to Xp11.3 microdeletion","OBSOLETE: Retinitis pigmentosa and intellectual disability due to del(X)(p11.3)"]},"uk":{"name":"ЗАСТАРІЛО: Пігментний ретиніт та розумова відсталість внаслідок моносомії Xp11.3","synonyms":["ЗАСТАРІЛО: Пігментна дегенерація сітківки та розумова відсталість внаслідок del(X)(p11.3)","ЗАСТАРІЛО: Пігментний ретиніт та розумова відсталість внаслідок мікроделеції Xp11.3"]},"zh":{"name":"弃用：Xp11.3单体所致视网膜色素变性和智力障碍","synonyms":["Xp11.3微缺失所致视网膜色素变性和智力障碍"]},"tr":{"name":"Eski adı: Retinitis pigmentosa ve monozomi Xp11.3'e bağlı zihinsel yetersizlik","synonyms":["Retinitis pigmentosa ve del (X) 'e bağlı zihinsel yetersizlik (p11.3)","Retinitis pigmentosa ve Xp11.3 mikrodelesyonuna bağlı zihinsel yetersizlik"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":85332,"name":"X-linked intellectual disability-retinitis pigmentosa syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}