is a rare, serious skin reaction causing painful rash and skin peeling.

is an inherited disorder affecting vision, hearing, joints, and facial development.

is an inherited disorder affecting vision, hearing, joints, and facial development.

is an inherited connective tissue disorder causing eye, hearing, and joint problems.

is a genetic connective tissue disorder affecting eyes, ears, joints, and face.

is a rare neurological disorder causing painful muscle stiffness and spasms.

is a rare genetic connective tissue disorder causing hard, thick skin.

is a rare neurological disorder causing painful muscle stiffness and spasms.

is a very rare genetic condition affecting growth, bones, and development.

is a rare genetic autoinflammatory disease causing infant-onset skin and lung damage.

is a cancer where stomach cells grow uncontrollably, often silently.

is a stomach cancer that can affect digestion, appetite, and overall health.

is an early-stage stomach cancer confined to the stomach's inner lining.

is a common term for conditions affecting the stomach and digestion.

is a condition where small pouches form in the stomach lining.

is inflammation of the mouth that can cause painful sores and swelling.

is a bladder pouch containing a stone that may cause urinary problems.

is a common, harmless pink birthmark often seen on newborns.

is a rare genetic disorder affecting muscles, bleeding, and several organs.

is an eye misalignment causing double vision and reduced depth perception.

is a rare birth defect where the mitral valve spans both ventricles.

is a rare heart valve defect where the tricuspid valve sits abnormally.

is a usually harmless change causing a speckled, cholesterol-studded gallbladder lining.

is a rare bacterial infection spread by rats or contaminated food.