B-lymphoblastic leukemia/lymphoma

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B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2)

ORPHA:585909Etiological subtype

Also called B-ALL with t(9;22)(q34.1;q11.2) · BCR-ABL1-like B-ALL · Philadelphia chromosome-like B-ALL

What it is

Orphanet has not published a description for this disease yet. The identifiers, classification and cross-references below are still current.

Key facts

Age of onset
Adolescent, Adult, Childhood, Elderly, Infancy
Inheritance
Not applicable
Classified as
Etiological subtype

Genes

FLT3Disease-causing somatic mutation(s)
HLA-CMajor susceptibility factor
ABL1Part of a fusion gene
BCRPart of a fusion gene
CDKN2ABiomarker tested
IKZF1Biomarker tested
TP53Biomarker tested

ICD-10 codes

C91.0filed under a broader ICD-10 category — shared with 9 other rare diseases

ICD-10 has no distinct code for most rare diseases, so many are filed under the nearest available one. A shared code identifies the group, not this disease — the ORPHAcode above is what identifies it.

Related health topics

Reached through the ICD-10 categories this disease is filed under, so these describe the broader group rather than this disease specifically.

Cross-references

MONDO 0035940UMLS C5680319

Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.

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