{"orpha":209016,"name":"Hematological disease associated with an acquired peripheral neuropathy","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-209016/","orphanet_url":"https://www.orpha.net/en/disease/detail/209016","names":{"fr":{"name":"Maladie hématologique avec neuropathie périphérique acquise"},"de":{"name":"Hämatologische Krankheit mit erworbener peripherer Neuropathie"},"es":{"name":"Enfermedad hematológica asociada con una neuropatía periférica adquirida"},"it":{"name":"Malattia ematologica associata a neuropatia periferica acquisita"},"nl":{"name":"Hematologische ziekte geassocieerd met verworven perifere neuropathie"},"pt":{"name":"Doença hematológica associada a uma neuropatia periférica adquirida"},"pl":{"name":"Choroba hematologiczna z towarzyszącą nabytą neuropatią obwodową"},"cs":{"name":"Hematologická onemocnění asociovaná se získanou periferní neuropatií"},"uk":{"name":"Гематологічне захворювання, повязане з набутою периферичною нейропатією"},"zh":{"name":"与获得性周围神经病变相关的血液疾病"},"tr":{"name":"Edinsel periferik nöropati ilişkili hematolojik hastalık"}},"xrefs":[{"source":"MONDO","code":"16180","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5680846","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":97992,"name":"Rare hematologic disease"},"parents":[{"orpha":182086,"name":"Acquired peripheral neuropathy","classifications":[181]}],"children":[{"orpha":207046,"name":"Malignant lymphoma with peripheral neuropathy","type":"Category"},{"orpha":29073,"name":"Multiple myeloma","type":"Disease"},{"orpha":2905,"name":"POEMS syndrome","type":"Disease"},{"orpha":86855,"name":"Plasmacytoma","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}