is a cancer (carcinoma) of the digestive tract and organs.

is a cancer of the digestive system’s lymphatic tissues.

is a usually slow-growing, noncancerous tumor arising from gut neuroendocrine cells.

is a rare, slow-growing tumor that starts in hormone-making digestive cells.

is a rare digestive tract cancer, often in stomach or small intestine.

is a noncancerous growth in the digestive system.

is cancer affecting digestive organs such as the stomach, bowel, or pancreas.

is a group of conditions affecting digestion, from the esophagus to intestines.

is a form of tuberculosis that affects the stomach or intestines.

is a rare bacterial infection causing fever, belly pain, vomiting, and diarrhea.

is an ulcer where the stomach and small intestine are joined.

is delayed stomach emptying without blockage, causing nausea, vomiting, and fullness.

is a birth defect where the intestines develop outside the baby’s belly.

is an inherited enzyme deficiency causing spleen enlargement, bone pain, anemia.

is an inherited disorder causing fatty substance buildup in organs and bones.

is a severe inherited disorder causing early brain and organ damage.

is a rare inherited disorder affecting organs, bones, and the brain.

is an inherited disorder with Gaucher features, eye weakness, and heart calcifications.

is a rare genetic condition causing unusually high glucagon hormone levels.

is a rare inherited eye disorder causing corneal clouding and vision loss.

is a rare genetic disorder causing short stature, stiff joints, heart problems.

is a rare genetic disorder causing short stature, joint stiffness, cardiac-airway complications.

is a rare genetic disorder causing short stature, joint stiffness, heart-lung complications.

is a rare genetic growth disorder causing short stature and stiff joints.