{"orpha":178996,"name":"Acquired neutropenia","type":"Category","group":"Group of disorders","status":"active","flags":[],"synonyms":["Immunologic neutropenia"],"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-178996/","orphanet_url":"https://www.orpha.net/en/disease/detail/178996","names":{"fr":{"name":"Neutropénie acquise","synonyms":["Neutropénie immunologique"]},"de":{"name":"Neutropenie, erworbene","synonyms":["Neutropenie, immunologische"]},"es":{"name":"Neutropenia adquirida","synonyms":["Neutropenia inmunológica"]},"it":{"name":"Neutropenia acquisita"},"nl":{"name":"Verworven neutropenie","synonyms":["Immunologische neutropenie"]},"pt":{"name":"Neutropenia adquirida"},"pl":{"name":"Neutropenia nabyta","synonyms":["Neutropenia immunologiczna"]},"cs":{"name":"Získaná neutropenie","synonyms":["Imunologicky podmíněná neutropenie"]},"uk":{"name":"Набута нейтропенія","synonyms":["Імунологічна нейтропенія"]},"zh":{"name":"获得性中性粒细胞减少症","synonyms":["免疫中性粒细胞减少症"]},"tr":{"name":"Edinsel nötropeni","synonyms":["İmmünolojik nötropeni"]}},"xrefs":[{"source":"ICD-11","code":"4B00.01","qualifier":"E","icd_relation":"specific","validated":true,"icd11_uri":"348671706"},{"source":"MONDO","code":"15822","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C4543729","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":98004,"name":"Rare immune disease"},"parents":[{"orpha":310050,"name":"Rare acquired immunodeficiency","classifications":[195]}],"children":[{"orpha":2688,"name":"Adult idiopathic neutropenia","type":"Disease"},{"orpha":47612,"name":"Felty syndrome","type":"Disease"},{"orpha":464370,"name":"Neonatal alloimmune neutropenia","type":"Disease"},{"orpha":86872,"name":"T-cell large granular lymphocyte leukemia","type":"Disease"}],"genes":[],"genes_via_subtypes":[],"inheritance":[],"onset":[],"prevalence":[],"phenotypes":null}