{"orpha":352699,"name":"OBSOLETE: Cobblestone lissencephaly type C","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":["OBSOLETE: Lissencephaly type 2C"],"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-352699/","orphanet_url":"https://www.orpha.net/en/disease/detail/352699","names":{"fr":{"name":"OBSOLETE : Lissencéphalie pavimenteuse type C","synonyms":["OBSOLETE : Lissencéphalie type 2C"]},"de":{"name":"OBSOLET: Cobblestone-Lissenzephalie Typ C","synonyms":["OBSOLET: Lissenzephalie Typ 2C"]},"es":{"name":"OBSOLETO: Lisencefalia en empedrado tipo C","synonyms":["OBSOLETO: Lisencefalia tipo 2C"]},"it":{"name":"OBSOLETO: Lissencefalia con aspetto ciottolato, tipo C","synonyms":["OBSOLETO: Lissencefalia, tipo 2C"]},"nl":{"name":"OBSOLEET: Cobblestone-lissencefalie type C","synonyms":["OBSOLEET: Lissencefalie type 2C"]},"pt":{"name":"OBSOLETO: Lissencefalia em pedra de calçada tipo C"},"pl":{"name":"NIEAKTUALNE: Lizencefalia typu kostki brukowej typu C","synonyms":["NIEAKTUALNE: Lizencefalia typu 2C"]},"cs":{"name":"NEAKTUÁLNÍ: Dlážděná lissencefalie typu C","synonyms":["OBSOLETE: Lissencephaly type 2C"]},"uk":{"name":"ЗАСТАРІЛО: Бруківкова лісенцефалія, тип С","synonyms":["ЗАСТАРІЛО: Лісенцефалія типу 2С"]},"zh":{"name":"弃用：鹅卵石样无脑畸形C型","synonyms":["无脑回畸形2C型"]},"tr":{"name":"Eski adı: Arnavut kaldırımı lizensefali tip C","synonyms":["Lissensefali tip 2C"]}},"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}