{"orpha":73220,"name":"X-linked intellectual disability-hypotonic face syndrome","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 Alpha-thalassemia-X-linked intellectual disability syndrome","url":"https://raremap.alftech.space/d/ORPHA-73220/","orphanet_url":"https://www.orpha.net/en/disease/detail/73220","names":{"fr":{"name":"Syndrome de déficience intellectuelle liée à l'X-faciès hypotonique"},"de":{"name":"X-chromosomale Intelligenzminderung-Syndrom-hypotones Gesicht-Syndrom"},"es":{"name":"Síndrome de discapacidad intelectual ligada al cromosoma X-rostro hipotónico"},"it":{"name":"Sindrome da disabilità intellettiva e facies ipotonica legata all'X"},"nl":{"name":"X-gebonden intellectuele achterstand - hypotoon aangezicht-syndroom"},"pt":{"name":"Síndrome de perturbação do desenvolvimento intelectual ligada ao X-hipotonia facial"},"pl":{"name":"Niepełnopsrawność intelektualna sprzężona z chromosomem X - hipotnia twarzy"},"cs":{"name":"Syndrom zahrnující X-vázanou mentální retardaci a hypotonický obličej"},"uk":{"name":"Х-зчеплений синдром розумової відсталості-гіпотонічного обличчя"},"zh":{"name":"X连锁智力低下-低张力面容综合征"},"tr":{"name":"X'e bağlı zihinsel yetersizlik-hipotonik yüz sendromu"}},"xrefs":[{"source":"OMIM","code":"309580","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":847,"name":"X-linked alpha-thalassemia-intellectual disability syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}