{"orpha":228340,"name":"OBSOLETE: CLN4A 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 CLN6 disease","url":"https://raremap.alftech.space/d/ORPHA-228340/","orphanet_url":"https://www.orpha.net/en/disease/detail/228340","names":{"fr":{"name":"OBSOLETE : Maladie CLN4A"},"de":{"name":"OBSOLET: CLN4A-Krankheit"},"es":{"name":"OBSOLETO: Enfermedad CLN4A"},"it":{"name":"OBSOLETO: Malattia CLN4A"},"nl":{"name":"OBSOLEET: CLN4A-ziekte"},"pt":{"name":"OBSOLETO: Doença CLN4A"},"pl":{"name":"NIEAKTUALNE: Choroba CLN4A"},"cs":{"name":"NEAKTUÁLNÍ: Neuronální ceroidlipofuscinosa, typ 4"},"uk":{"name":"ЗАСТАРІЛО: Хвороба CLN4A"},"zh":{"name":"神经元蜡样脂褐质沉积症4A型"},"tr":{"name":"CLN4A hastalığı"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":228363,"name":"CLN6 disease"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}