is an aggressive blood cancer driven by BCR-ABL1 (Philadelphia chromosome).

is a childhood blood cancer with ETV6-RUNX1 fusion, usually favorable prognosis.

is a blood cancer of immature B cells with extra chromosomes (hyperdiploidy).

is a fast-growing blood and lymph cancer with too few chromosomes (hypodiploidy).

is a fast-growing blood cancer with chromosome 21 amplification (iAMP21) subtype.

is a fast-growing blood cancer of immature B cells, involving IL3-IGH.

is a blood cancer of immature B cells with recurrent genetic changes.

is a fast-growing blood cancer of immature B cells.

is a childhood blood cancer with ETV6-RUNX1 (t(12;21)) fusion.

is a rare, aggressive B-cell blood cancer with chromosome 17;19 translocation.

is a rare blood cancer linked to chromosome t(5;14) translocation.

is a rare genetic subtype of leukemia/lymphoma affecting immature B cells.

is a fast-growing B-cell blood cancer with Philadelphia chromosome (BCR-ABL1).

is a rare, aggressive leukemia/lymphoma driven by KMT2A (11q23) rearrangements.

is a fast-growing cancer of immature B cells with TCF3-PBX1 fusion.

is a high-risk subtype of B-cell acute lymphoblastic leukemia.

is a rare genetic connective tissue disorder with skeletal abnormalities and hypermobility.

is a rare inherited disorder of protein glycosylation affecting multiple organs.

is a rare genetic connective tissue disorder with short stature and hypermobility.

is a degenerative lumbar condition where spinous processes touch, causing back pain.

is a tick-borne parasitic infection of red blood cells, causing flu-like illness.

is a bacterial infection causing skin and organ lesions in immunocompromised people.

is early diabetic eye damage to the retina, often without symptoms.

is a contagious eye infection causing redness, discharge, and crusted eyelids.