{"orpha":514980,"name":"ATP13A2-related parkinsonism","type":"Clinical group","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-514980/","orphanet_url":"https://www.orpha.net/en/disease/detail/514980","names":{"fr":{"name":"Parkinsonisme associé à ATP13A2"},"de":{"name":"ATP13A2-assoziierter Parkinsonismus"},"es":{"name":"Parkinsonismo asociado a ATP13A2"},"it":{"name":"Parkinsonismo ATP13A2-correlato"},"nl":{"name":"ATP13A2-gerelateerd parkinsonisme"},"pt":{"name":"Parkinsonismo ATP13A2-relacionado"},"pl":{"name":"ATP13A2-związany z chorobą Parkinsona"},"cs":{"name":"ATP13A2-vázaný parkinsonismus"},"uk":{"name":"Паркінсонізм, повязаний з ATP13A2"},"zh":{"name":"ATP13A2基因相关帕金森病"},"tr":{"name":"ATP13A2-ilişkili parkinsonizm"}},"xrefs":[{"source":"UMLS","code":"C5681397","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":307055,"name":"Rare parkinsonian syndrome due to genetic neurodegenerative disease","classifications":[156]},{"orpha":306666,"name":"Rare parkinsonian syndrome due to neurodegenerative disease","classifications":[181]}],"children":[{"orpha":314632,"name":"CLN12 disease","type":"Disease"},{"orpha":306674,"name":"Kufor-Rakeb syndrome","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":["Adolescent","Childhood"],"prevalence":[{"type":"Point prevalence","qualification":"Class only","class":"<1 / 1 000 000","value":0.0,"area":"Worldwide","status":"Validated","source":"ORPHANET_22388936[PMID]_29112700[PMID]"}],"phenotypes":null}