{"orpha":83648,"name":"OBSOLETE: X-linked recessive intellectual disability-macrocephaly-ciliary dysfunction syndrome","type":"Disease","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 Multiple congenital anomalies-hypotonia-seizures syndrome type 2","url":"https://raremap.alftech.space/d/ORPHA-83648/","orphanet_url":"https://www.orpha.net/en/disease/detail/83648","names":{"fr":{"name":"OBSOLETE : Syndrome de déficience intellectuelle récessive liée à l'X-macrocéphalie-dysfonction ciliaire"},"de":{"name":"OBSOLET: X-chromosomal-rezessive Intelligenzminderung-Makrozephalie-Ziliendysfunktion-Syndrom"},"es":{"name":"OBSOLETO: Síndrome de discapacidad intelectual recesiva ligada al cromosoma X-macrocefalia-disfunción ciliar"},"it":{"name":"OBSOLETO: Ritardo mentale recessivo legato all'X - macrocefalia - disfunzione ciliare"},"nl":{"name":"OBSOLEET: X-gebonden recessieve intellectuele achterstand - macrocefalie - ciliaire disfunctie-syndroom"},"pt":{"name":"OBSOLETO: Síndrome de perturbação do desenvolvimento intelectual ligada ao X recessiva-macrocefalia-disfunção ciliar"},"pl":{"name":"NIEAKTUALNE: Recesywna niepelnosprawnosc intelektualna sprzezona z chromosomem X - makrocefalia - dysfunkcja rzesek"},"cs":{"name":"NEAKTUÁLNÍ: X-vázaný recesivní syndrom zahrnující mentální retardaci, makrocefalii a ciliární dysfunkci"},"uk":{"name":"Х-зчеплений рецесивний синдром інтелектуальної недостатності-макроцефалії-циліарної дисфункції"},"zh":{"name":"弃用：X连锁隐性智力障碍-大头畸形-纤毛功能障碍综合征"},"tr":{"name":"Eski adı: X'e bağlı resesif zihinsel yetersizlik-makrosefali-siliyer disfonksiyon sendromu"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":300496,"name":"Multiple congenital anomalies-hypotonia-seizures syndrome type 2"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}