{"orpha":641375,"name":"B-lymphoblastic leukemia/lymphoma with t(17;19)","type":"Etiological subtype","group":"Subtype of disorder","status":"active","flags":[],"synonyms":[],"definition":null,"note":null,"url":"https://raremap.alftech.space/d/ORPHA-641375/","orphanet_url":"https://www.orpha.net/en/disease/detail/641375","names":{"fr":{"name":"Leucémie/lymphome lymphoblastique B associé à t(17;19)"},"de":{"name":"B-lymphoblastische Leukämie/Lymphom mit t(17;19)"},"es":{"name":"Leucemia/linfoma linfoblástico de células B con t(17;19)"},"it":{"name":"Leucemia linfoblastica a cellule B/linfoma con t(17;19)"},"nl":{"name":"B-lymfoblastische leukemie/lymfoom met t(17;19)"},"pt":{"name":"Leucemia linfoblástica B/linfoma com t(17;19)"},"pl":{"name":"Białaczka/chłoniak limfoblastyczny z komórek B z t(17;19)"},"cs":{"name":"B-lymfoblastická leukemie/lymfom s t(17;19)"},"uk":{"name":"В-лімфобластний лейкоз/лімфома з t(17;19)"}},"xrefs":[{"source":"ICD-11","code":"2A70.Y","qualifier":"NTBT","icd_relation":"attributed","validated":true,"icd11_uri":"null"},{"source":"MONDO","code":"0957428","qualifier":"E","icd_relation":null,"validated":true},{"source":"UMLS","code":"C5816789","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":"HLF","name":"HLF transcription factor, PAR bZIP family member","gene_type":"gene with protein product","association":"Part of a fusion gene in","status":"Assessed","source":"20519628[PMID]","hgnc":"4977","ensembl":"ENSG00000108924","omim":"142385","loci":["17q22"]},{"symbol":"TCF3","name":"transcription factor 3","gene_type":"gene with protein product","association":"Part of a fusion gene in","status":"Assessed","source":"23346431[PMID]","hgnc":"11633","ensembl":"ENSG00000071564","omim":"147141","loci":["19p13.3"]}],"genes_via_subtypes":[],"inheritance":["Not applicable"],"onset":[],"prevalence":[],"phenotypes":null}