{"orpha":101052,"name":"OBSOLETE: Microlissencephaly type B","type":"Disease","group":"Disorder","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"definition":null,"note":"This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Microlissencephaly","url":"https://raremap.alftech.space/d/ORPHA-101052/","orphanet_url":"https://www.orpha.net/en/disease/detail/101052","names":{"fr":{"name":"OBSOLETE : Microlissencéphalie type B"},"de":{"name":"OBSOLET: Mikrolissenzephalie Typ B"},"es":{"name":"OBSOLETO: Microlisencefalia tipo B"},"it":{"name":"OBSOLETO: Microlissencefalia, tipo B"},"nl":{"name":"OBSOLEET: Microlissencefalie type B"},"pt":{"name":"OBSOLETO: Microlisencefalia, tipo B"},"pl":{"name":"NIEAKTUALNE: Mikrolizencefalia typu B"},"cs":{"name":"NEAKTUÁLNÍ: Mikrolissencefalie typu B"},"uk":{"name":"ЗАСТАРІЛО: Мікролісенцефалія, тип В"},"zh":{"name":"弃用：小头畸形B型"},"tr":{"name":"Eski adı: Mikrolizensefali tip B"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":1083,"name":"Microlissencephaly"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}