{"orpha":102369,"name":"Rare syndromic intellectual disability","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.","url":"https://raremap.alftech.space/d/ORPHA-102369/","orphanet_url":"https://www.orpha.net/en/disease/detail/102369","names":{"fr":{"name":"Déficience intellectuelle syndromique rare"},"de":{"name":"Seltene syndromale Intelligenzminderung"},"es":{"name":"Discapacidad intelectual rara sindrómica"},"it":{"name":"Disabilità intellettiva sindromica rara"},"nl":{"name":"Zeldzame syndromale intellectuele achterstand"},"pt":{"name":"Perturbação do desenvolvimento intelectual sindromática rara"},"pl":{"name":"Rzadka niepełnosprawność intelektualna z wadą rozwojową","synonyms":["Syndromiczna niepełnosprawność intelektualna","Syndromiczna niepełnosprawność umysłowa"]},"cs":{"name":"Vzácné syndromické mentální retardace"},"uk":{"name":"Рідкісна синдромна розумова відсталість"},"zh":{"name":"罕见综合征性智力障碍"},"tr":{"name":"Nadir sendromik zihinsel yetersizlik"}},"xrefs":[{"source":"MONDO","code":"15162","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5681780","qualifier":"E","icd_relation":null,"validated":true},{"source":"GARD","code":"19834","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":2156,"name":"OBSOLETE: Hirsutism-skeletal dysplasia-intellectual disability syndrome","status":"inactive"},{"type":"Referred to","orpha":2580,"name":"OBSOLETE: Shoulder and girdle defects-familial intellectual disability syndrome","status":"inactive"},{"type":"Referred to","orpha":2861,"name":"OBSOLETE: Short stature-microcephaly-heart defect syndrome","status":"inactive"},{"type":"Referred to","orpha":3043,"name":"OBSOLETE: Intellectual disability-unusual facies syndrome","status":"inactive"},{"type":"Referred to","orpha":3046,"name":"OBSOLETE: Intellectual disability-unusual facies, Davis-Lafer type","status":"inactive"},{"type":"Referred to","orpha":3050,"name":"OBSOLETE: Intellectual disability-hypotonia-skin hyperpigmentation syndrome","status":"inactive"},{"type":"Referred to","orpha":3064,"name":"OBSOLETE: X-linked intellectual disability, Wittner type","status":"inactive"},{"type":"Referred to","orpha":3360,"name":"OBSOLETE: Trichodermal syndrome-intellectual disability syndrome","status":"inactive"},{"type":"Referred to","orpha":85318,"name":"OBSOLETE: X-linked intellectual disability-precocious puberty-obesity syndrome","status":"inactive"},{"type":"Referred to","orpha":98464,"name":"OBSOLETE: X-linked syndromic intellectual disability","status":"inactive"},{"type":"Referred to","orpha":182073,"name":"OBSOLETE: Syndromic neurometabolic disease with non-X-linked intellectual disability","status":"inactive"},{"type":"Referred to","orpha":182076,"name":"OBSOLETE: Syndromic neurometabolic disease with X-linked intellectual disability","status":"inactive"},{"type":"Referred to","orpha":371054,"name":"OBSOLETE: X-linked congenital disorder of glycosylation with intellectual disability as a major feature","status":"inactive"},{"type":"Referred to","orpha":371064,"name":"OBSOLETE: Non-X-linked congenital disorder of glycosylation with intellectual disability as a major feature","status":"inactive"}],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":87277,"name":"Rare intellectual disability","classifications":[181]}],"children":[{"orpha":102283,"name":"Multiple congenital anomalies/dysmorphic syndrome-intellectual disability","type":"Category"},{"orpha":611314,"name":"Rare syndromic intellectual disability without multiple congenital anomalies/dysmorphic syndrome","type":"Category"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}