{"orpha":209010,"name":"Peripheral neuropathy associated with monoclonal gammopathy","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":[],"definition":null,"note":"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.","url":"https://raremap.alftech.space/d/ORPHA-209010/","orphanet_url":"https://www.orpha.net/en/disease/detail/209010","names":{"fr":{"name":"Neuropathie périphérique avec gammopathie monoclonale"},"de":{"name":"Periphere Neuropathie mit assoziierter monoklonaler Gammopathie"},"es":{"name":"Neuropatía periférica asociada con gammopatía monoclonal"},"it":{"name":"Neuropatia periferica associata a gammopatia monoclonale"},"nl":{"name":"Perifere neuropathie geassocieerd met monoklonale gammopathie"},"pt":{"name":"Neuropatia periférica associada com gamapatia monoclonal"},"pl":{"name":"Neuropatia obwodowa związana z gammopatią monoklonalną"},"cs":{"name":"Periferní neuropatie asociovaná s monoklonální gamapatií"},"uk":{"name":"Периферична нейропатія, повязана з моноклональною гамма-патією"},"zh":{"name":"单克隆丙种球蛋白病相关的周围神经病变"},"tr":{"name":"Monoklonal gammopati ilişkili periferik nöropati"}},"xrefs":[{"source":"MONDO","code":"16178","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680821","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[{"type":"Referred to","orpha":208981,"name":"OBSOLETE: Polyradiculoneuropathy associated with IgG/IgA/IgM monoclonal gammopathy without known antibodies","status":"inactive"}],"preferential_parent":{"orpha":98006,"name":"Rare neurologic disease"},"parents":[{"orpha":182086,"name":"Acquired peripheral neuropathy","classifications":[181]}],"children":[{"orpha":71279,"name":"CANOMAD syndrome","type":"Disease"},{"orpha":2905,"name":"POEMS syndrome","type":"Disease"},{"orpha":209004,"name":"Polyneuropathy associated with IgM monoclonal gammopathy","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}