ORPHA:641372

B-lymphoblastic leukemia/lymphoma with t(7;9)(q11.2;p13.2)

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(7;9)(q11.2;p13.2)
fr	Leucémie/lymphome lymphoblastique B associé à t(7;9)(q11.2;p13.2)
de	B-lymphoblastische Leukämie/Lymphom mit t(7;9)(q11.2;p13.2)
es	Leucemia/linfoma linfoblástico de células B con t(7;9)(q11.2;p13.2)
it	Leucemia linfoblastica a cellule B/linfoma con t(7;9)(q11.2;p13.2)
nl	B-lymfoblastische leukemie/lymfoom met t(7;9)(q11.2;p13.2)
pt	Leucemia linfoblástica B/linfoma com t(7;9)(q11.2;p13.2)
pl	Białaczka/chłoniak limfoblastyczny z komórek B z t(7;9)(q11.2;p13.2)
cs	B-lymfoblastická leukemie/lymfom s t(7;9)(q11.2;p13.2)
uk	В-лімфобластний лейкоз/лімфома з t(7;9)(q11.2;p13.2)

qualifier = Orphanet mapping relation

Source	Code	Qualifier	ICD relation	Validation
ICD-11	2A70.Y	NTBT	attributed	validated
MONDO	0957427	E		validated
UMLS	C5816790	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
AUTS2	Part of a fusion gene in	Assessed	HGNC:14262	ENSG00000158321	607270	7q11.22	activator of transcription and developmental regulator AUTS2	22578776[PMID]
PAX5	Part of a fusion gene in	Assessed	HGNC:8619	ENSG00000196092	167414	9p13.2	paired box 5	21962897[PMID]_22578776[PMID]_17179230[PMID]

0 records

No prevalence record in this release.

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