ORPHA:641375

B-lymphoblastic leukemia/lymphoma with t(17;19)

Orphadata ships no English definition for this code.

Names in Orphadata languages

10 of 12 languages

Lang	Name	Synonyms
en	B-lymphoblastic leukemia/lymphoma with t(17;19)
fr	Leucémie/lymphome lymphoblastique B associé à t(17;19)
de	B-lymphoblastische Leukämie/Lymphom mit t(17;19)
es	Leucemia/linfoma linfoblástico de células B con t(17;19)
it	Leucemia linfoblastica a cellule B/linfoma con t(17;19)
nl	B-lymfoblastische leukemie/lymfoom met t(17;19)
pt	Leucemia linfoblástica B/linfoma com t(17;19)
pl	Białaczka/chłoniak limfoblastyczny z komórek B z t(17;19)
cs	B-lymfoblastická leukemie/lymfom s t(17;19)
uk	В-лімфобластний лейкоз/лімфома з t(17;19)

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-11	2A70.Y	NTBT	attributed	validated
MONDO	0957428	E		validated
UMLS	C5816789	E		validated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

ORPHA:99860Precursor B-cell acute lymphoblastic leukemia
rare hematological diseases; rare neoplastic diseases; rare transplant-related disorders

No children.

2 direct

Gene	Association	Status	HGNC	Ensembl	OMIM	Locus	Name	Source of validation
HLF	Part of a fusion gene in	Assessed	HGNC:4977	ENSG00000108924	142385	17q22	HLF transcription factor, PAR bZIP family member	20519628[PMID]
TCF3	Part of a fusion gene in	Assessed	HGNC:11633	ENSG00000071564	147141	19p13.3	transcription factor 3	23346431[PMID]

0 records

No prevalence record in this release.

Orphanet has no HPO annotation for this code in this release.