is a rare infant leukemia affecting megakaryoblasts (platelet-forming cells).

is a rare, aggressive blood cancer with a specific chromosome change.

is a rare, aggressive leukemia defined by a specific chromosome change.

is a rare, aggressive leukemia of white blood cell precursors.

is a leukemia subtype defined by RUNX1-RUNX1T1 fusion and favorable prognosis.

is a leukemia subtype with t(8;21) genetic fusion, often favorable prognosis.

is a blood cancer characterized by KMT2A rearrangement, often monocytic, intermediate risk.

is a rare, aggressive blood cancer with BCR-ABL1 gene fusion (Philadelphia chromosome).

is a fast-growing blood cancer of white blood-forming (myeloid, monocytic) cells.

is a heart attack from sudden coronary artery blockage, damaging heart muscle.

is sudden heart muscle inflammation causing chest pain, shortness of breath, arrhythmias.

is a rare, severe brain inflammation causing rapid swelling and tissue damage.

is a rare, rapidly progressive brain disorder in children after viral infections.

is sudden, severe pancreatic inflammation causing tissue death and life-threatening complications.

is a rare urea cycle disorder causing life-threatening newborn ammonia buildup.

is a potentially life-threatening overdose causing slowed breathing and unconsciousness.

is sudden eye socket tissue inflammation causing pain, swelling, and vision problems.

is sudden pancreas inflammation causing severe abdominal pain and digestive problems.

is a rare disorder causing sudden autonomic (involuntary) nervous system failure.

is a rare, aggressive bone marrow cancer causing scarring and low counts.

is sudden inflammation around a tooth root causing pain and chewing tenderness.

is a painful, swollen infection of ear cartilage, often after piercing.

is sudden limb artery blockage (ischemia) reducing blood flow and risking tissue.

involves overdose of certain medicines affecting heart and nerves, requiring emergency treatment.