{"orpha":352694,"name":"OBSOLETE: Cobblestone lissencephaly type A","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Lissencephaly type 2A"],"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 Congenital muscular alpha-dystroglycanopathy with brain and eye anomalies","url":"https://raremap.alftech.space/d/ORPHA-352694/","orphanet_url":"https://www.orpha.net/en/disease/detail/352694","names":{"fr":{"name":"OBSOLETE : Lissencéphalie pavimenteuse type A","synonyms":["OBSOLETE : Lissencéphalie type 2A"]},"de":{"name":"OBSOLET: Cobblestone-Lissenzephalie Typ A","synonyms":["OBSOLET: Lissenzephalie Typ 2A"]},"es":{"name":"OBSOLETO: Lisencefalia en empedrado tipo A","synonyms":["OBSOLETO: Lisencefalia tipo 2A"]},"it":{"name":"OBSOLETO: Lissencefalia con aspetto ciottolato tipo A","synonyms":["OBSOLETO: Lissencefalia, tipo 2A"]},"nl":{"name":"OBSOLEET: Cobblestone-lissencefalie type A","synonyms":["OBSOLEET: Lissencefalie type 2A"]},"pt":{"name":"OBSOLETO: Lissencefalia em pedra de calçada tipo A"},"pl":{"name":"NIEAKTUALNE: Lizencefalia typu kostki brukowej typu A","synonyms":["NIEAKTUALNE: Lizencefalia typu 2A"]},"cs":{"name":"NEAKTUÁLNÍ: Dlážděná lissencefalie typu A","synonyms":["OBSOLETE: Lissencephaly type 2A"]},"uk":{"name":"ЗАСТАРІЛО: Бруківкова лісенцефалія, тип А","synonyms":["ЗАСТАРІЛО: Лісенцефалія типу 2А"]},"zh":{"name":"弃用：鹅卵石样无脑畸形A型","synonyms":["无脑回畸形2A型"]},"tr":{"name":"Eski adı: Arnavut kaldırımı lizensefali tip A","synonyms":["Lissensefali tip 2A"]}},"xrefs":[],"associations":[{"type":"Referred to","orpha":352687,"name":"Congenital muscular alpha-dystroglycanopathy with brain and eye anomalies"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}