{"orpha":182076,"name":"OBSOLETE: Syndromic neurometabolic disease with X-linked intellectual disability","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Rare syndromic intellectual disability","url":"https://raremap.alftech.space/d/ORPHA-182076/","orphanet_url":"https://www.orpha.net/en/disease/detail/182076","names":{"fr":{"name":"OBSOLETE : Maladie neurométabolique syndromique avec déficience intellectuelle liée à l'X"},"de":{"name":"OBSOLET: Syndromale neurometabolische Krankheit mit X-chromosomaler Intelligenzminderung"},"es":{"name":"OBSOLETO: Enfermedad neurometabólica sindrómica con discapacidad intelectual ligada al cromosoma X"},"it":{"name":"OBSOLETO: Malattia neurometabolica sindromica associata a disabilità intellettiva legata all'X"},"nl":{"name":"OBSOLEET: Syndromale neurometabole ziekte met X-gebonden intellectuele achterstand"},"pt":{"name":"OBSOLETO: Doença neurometabólica sindromática com perturbação do desenvolvimento intelectual ligada ao X"},"pl":{"name":"NIEAKTUALNE: Syndromiczna choroba neurometaboliczna z niepełnosprawnością intelektualną sprzężoną z chromosomem X"},"cs":{"name":"NEAKTUÁLNÍ: Neurometabolická syndromická onemocnění s X-vázanou mentální retardací"},"uk":{"name":"ЗАСТАРІЛО: Синдромне нейрометаболічне захворювання зі зчепленою з Х-хромосомою розумовою відсталістю"},"zh":{"name":"综合征性神经代谢疾病伴X连锁智力障碍"},"tr":{"name":"X'e bağlı zihinsel yetersizlik ile seyreden sendromik nörometabolik hastalık"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":102369,"name":"Rare syndromic intellectual disability"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}