{"orpha":98697,"name":"OBSOLETE: Genetic keratinization disorder associated with ocular features","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 Inherited ichthyosis syndromic form","url":"https://raremap.alftech.space/d/ORPHA-98697/","orphanet_url":"https://www.orpha.net/en/disease/detail/98697","names":{"fr":{"name":"OBSOLETE : Trouble de la kératinisation avec atteintes oculaires"},"de":{"name":"OBSOLET: Keratinisierungsstörung mit assoziierter Augenbeteiligung, genetisch bedingt"},"es":{"name":"OBSOLETO: Trastorno genético de la queratinización asociado a manifestaciones oculares"},"it":{"name":"OBSOLETO: Disturbo genetico della cheratinizzazione associato a segni oculari"},"nl":{"name":"OBSOLEET: Genetische keratinisatiestoornis geassocieerd met oculaire kenmerken"},"pt":{"name":"OBSOLETO: Doença da queratinização associada a doença ocular genética"},"pl":{"name":"NIEAKTUALNE: Genetyczne zaburzenia rogowacenia z objawami ocznymi"},"cs":{"name":"NEAKTUÁLNÍ: Geneticky podmíněné poruchy keratinizace s očními příznaky"},"uk":{"name":"ЗАСТАРІЛО: Генетично обумовлене порушення кератинізації, повязане з особливостями очей"},"zh":{"name":"弃用：遗传性角化异常相关性眼特征"},"tr":{"name":"Eski adı: Oküler özelliklerle ilişkili genetik keratinizasyon bozukluğu"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":281085,"name":"Inherited ichthyosis syndromic form"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}