{"orpha":2679,"name":"OBSOLETE: Infantile axonal neuropathy","type":"Disease","group":"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 Genetic peripheral neuropathy","url":"https://raremap.alftech.space/d/ORPHA-2679/","orphanet_url":"https://www.orpha.net/en/disease/detail/2679","names":{"fr":{"name":"OBSOLETE : Neuropathie axonale infantile"},"de":{"name":"OBSOLET: Neuropathie, axonale infantile"},"es":{"name":"OBSOLETO: Neuropatía axonal infantil"},"it":{"name":"OBSOLETO: Neuropatia assonale infantile"},"nl":{"name":"OBSOLEET: Infantiele axonale neuropathie"},"pt":{"name":"OBSOLETO: Neuropatia axonal do lactente"},"pl":{"name":"NIEAKTUALNE: Dziecieca neuropatia aksonalna"},"cs":{"name":"NEAKTUÁLNÍ: Dětská axonální neuropatie"},"uk":{"name":"ЗАСТАРІЛО: Інфантильна аксональна нейропатія"},"zh":{"name":"弃用：小儿轴突性神经病"},"tr":{"name":"Eski adı: İnfantil aksonal nöropati"}},"xrefs":[],"associations":[{"type":"Referred to","orpha":98497,"name":"Genetic peripheral neuropathy"}],"incoming_associations":[],"preferential_parent":null,"parents":[],"children":[],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}