is a rare inherited disorder affecting glycosylation, development, and sometimes bleeding.

is a rare genetic disorder affecting brain development and sugar processing.

is a rare inherited connective tissue disorder affecting bones, joints, and skin.

is a rare genetic disorder affecting development, movement, and sugar processing.

is an inherited iron overload disorder caused by changes in SLC40A1.

is a condition that disrupts normal sleep quality, timing, or duration.

is a parasitic infection spread by tsetse flies that affects the brain.

is a rare genetic bone disorder causing unusually slender, fragile bones.

is a rare inherited disorder causing harmful sugar buildup in cells.

is a rare genetic condition that can affect development and overall health.

is a birth defect where part of the small intestine is blocked.

is a rare cancer of the small intestine's connective tissues.

is an aggressive cancer that often starts in the lungs.

is a rare, aggressive bladder cancer that often spreads quickly.

is a rare, aggressive ovarian cancer that usually affects younger people.

is a fast-growing lung cancer that often spreads early.

is a rare, aggressive bone cancer that makes abnormal bone tissue.

is a rare cancer made of small, abnormal cells, often aggressive.

is a rare gut tumor that makes excess glucagon-like peptide hormones.

is a rare cancer that starts in the small intestine.

is a rare tumor in the small intestine that releases VIP.

is a rare small bowel cancer that starts in the intestine’s lining.

is a noncancerous growth in the small intestine.

is a rare cancer that begins in the small intestine.