{"orpha":641372,"name":"B-lymphoblastic leukemia/lymphoma with t(7;9)(q11.2;p13.2)","type":"Etiological subtype","group":"Subtype of disorder","status":"active","flags":[],"synonyms":[],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-641372/","orphanet_url":"https://www.orpha.net/en/disease/detail/641372","names":{"fr":{"name":"Leucémie/lymphome lymphoblastique B associé à t(7;9)(q11.2;p13.2)"},"de":{"name":"B-lymphoblastische Leukämie/Lymphom mit t(7;9)(q11.2;p13.2)"},"es":{"name":"Leucemia/linfoma linfoblástico de células B con t(7;9)(q11.2;p13.2)"},"it":{"name":"Leucemia linfoblastica a cellule B/linfoma con t(7;9)(q11.2;p13.2)"},"nl":{"name":"B-lymfoblastische leukemie/lymfoom met t(7;9)(q11.2;p13.2)"},"pt":{"name":"Leucemia linfoblástica B/linfoma com t(7;9)(q11.2;p13.2)"},"pl":{"name":"Białaczka/chłoniak limfoblastyczny z komórek B z t(7;9)(q11.2;p13.2)"},"cs":{"name":"B-lymfoblastická leukemie/lymfom s t(7;9)(q11.2;p13.2)"},"uk":{"name":"В-лімфобластний лейкоз/лімфома з t(7;9)(q11.2;p13.2)"}},"xrefs":[{"source":"ICD-11","code":"2A70.Y","qualifier":"NTBT","icd_relation":"attributed","validated":true,"icd11_uri":"null"},{"source":"MONDO","code":"0957427","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5816790","qualifier":"E","icd_relation":null,"validated":true}],"associations":[],"incoming_associations":[],"preferential_parent":{"orpha":250908,"name":"Rare neoplastic disease"},"parents":[{"orpha":99860,"name":"Precursor B-cell acute lymphoblastic leukemia","classifications":[194,202,233]}],"children":[],"genes":[{"symbol":"AUTS2","name":"activator of transcription and developmental regulator AUTS2","gene_type":"gene with protein product","association":"Part of a fusion gene in","status":"Assessed","source":"22578776[PMID]","hgnc":"14262","ensembl":"ENSG00000158321","omim":"607270","loci":["7q11.22"]},{"symbol":"PAX5","name":"paired box 5","gene_type":"gene with protein product","association":"Part of a fusion gene in","status":"Assessed","source":"21962897[PMID]_22578776[PMID]_17179230[PMID]","hgnc":"8619","ensembl":"ENSG00000196092","omim":"167414","loci":["9p13.2"]}],"genes_via_subtypes":[],"inheritance":["Not applicable"],"onset":[],"prevalence":[],"phenotypes":null}