{"orpha":98296,"name":"OBSOLETE: Ichthyosis associated with a cornified cell envelope and epidermal lipid metabolism anomaly","type":"Category","group":"Group of disorders","status":"inactive","flags":["Obsolete entity"],"synonyms":[],"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 Ichthyosis","url":"https://raremap.alftech.space/d/ORPHA-98296/","orphanet_url":"https://www.orpha.net/en/disease/detail/98296","names":{"fr":{"name":"OBSOLETE : Ichtyose associée à une cornification de la membrane cellulaire et à une anomalie du métabolisme lipidique"},"de":{"name":"OBSOLET: Ichthyose mit assoziierter Anomalie der verhornten Zellhüllen und des epidermalen Lipid-Stoffwechsels"},"es":{"name":"OBSOLETO: Ictiosis asociada con una envoltura celular cornificada y con anomalías del metabolismo lipídico epidérmico"},"it":{"name":"OBSOLETO: Ittiosi associata ad anomalia dello strato di cellule cornificate e del metabolismo del lipidi epidermici"},"nl":{"name":"OBSOLEET: Ichthyosis geassocieerd met gehoornde celenvelop en anomalie van epidermaal vetmetabolisme"},"pt":{"name":"OBSOLETO: Ictiose associada a envelope celular cornificado e anomalia do metabolismo lipídico da epiderme"},"pl":{"name":"NIEAKTUALNE: Rybia luska z towarzyszaca otoczka zrogowaciala komórek i wada metabolizmu lipidów naskórka"},"cs":{"name":"NEAKTUÁLNÍ: Ichtyóza související s anomálií zrohovatělého buněčného obalu a epidermálního lipidového metabolismu"},"uk":{"name":"ЗАСТАРІЛО: Іхтіоз, повязаний з ороговілою клітинною оболонкою та аномалією епідермального метаболізму ліпідів"},"zh":{"name":"弃用：角质化包膜形成和表皮脂质代谢异常相关鱼鳞病"},"tr":{"name":"Eski adı: Kornifiye hücre zarfı ve epidermal lipid metabolizması anomalisi-ilişkili iktiyoz"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":79354,"name":"Ichthyosis"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}