{"orpha":228357,"name":"OBSOLETE: CLN9 disease","type":"Etiological subtype","group":"Subtype of 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 Neuronal ceroid lipofuscinosis","url":"https://raremap.alftech.space/d/ORPHA-228357/","orphanet_url":"https://www.orpha.net/en/disease/detail/228357","names":{"fr":{"name":"OBSOLETE : Maladie CLN9"},"de":{"name":"OBSOLET: CLN9-Krankheit"},"es":{"name":"OBSOLETO: Enfermedad CLN9"},"it":{"name":"OBSOLETO: Malattia CLN9"},"nl":{"name":"OBSOLEET: CLN9-ziekte"},"pt":{"name":"OBSOLETO: Doença CLN9"},"pl":{"name":"NIEAKTUALNE: Choroba CLN9"},"cs":{"name":"NEAKTUÁLNÍ: Neuronální ceroidlipofuscinosa, typ 9"},"uk":{"name":"ЗАСТАРІЛО: хвороба CLN9"},"zh":{"name":"神经元蜡样脂褐质沉积症9型"},"tr":{"name":"CLN9 hastalığı"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":216,"name":"Neuronal ceroid lipofuscinosis"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}