{"orpha":2829,"name":"Partington-Anderson 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 Cohen syndrome","url":"https://raremap.alftech.space/d/ORPHA-2829/","orphanet_url":"https://www.orpha.net/en/disease/detail/2829","names":{"fr":{"name":"Syndrome de Partington-Anderson"},"de":{"name":"Partington-Anderson-Syndrom"},"es":{"name":"Síndrome de Partington Anderson"},"it":{"name":"Sindrome di Partington-Anderson"},"nl":{"name":"Syndroom van Partington-Anderson"},"pt":{"name":"Síndrome Partington-Anderson"},"pl":{"name":"Zespół Partingtona i Andersona"},"cs":{"name":"Partingtonův-Andersonův syndrom","synonyms":["Partington-Andersonův syndrom"]},"uk":{"name":"Синдром Партингтона-Андерсона"},"zh":{"name":"Partington-Anderson综合征"},"tr":{"name":"Partington-Anderson sendromu"}},"xrefs":[{"source":"OMIM","code":"260555","qualifier":"E","icd_relation":null,"validated":true},{"source":"MeSH","code":"C536299","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C1850075","qualifier":"E","icd_relation":null,"validated":true}],"associations":[{"type":"Moved to","orpha":193,"name":"Cohen syndrome"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}