Leukemia, acute lymphoblastic, susceptibility to, 3

Summary

An inherited condition caused by mutation(s) in the PAX5 gene, encoding paired box protein Pax-5. The condition is characterized by an increased risk of developing B-cell acute lymphoblastic leukemia. [from NCI]

Available tests

17 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (17 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

Associated genes Help
Genes reported to contribute to the condition.

PAX5
80 tests
Also known as: ALL3, BSAP, PAX-5, PAX5
Summary: paired box 5

Reviews

Clinical resources

Molecular resources

Consumer resources

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