is a rare inherited disorder causing heart, spine, wrist, and facial anomalies.

is a rare, often aggressive cancer of heart or blood vessels.

is a noncancerous growth in the heart or blood vessels.

is a late syphilis complication damaging the aorta and heart valves.

is a group of heart and blood vessel disorders affecting circulation.

is a genetic disorder causing facial weakness, low muscle tone, feeding problems.

is a progressive movement disorder causing parkinsonism, linked to tropical plant toxins.

is a genetic syndrome causing benign tumors, skin spots, and hormone overactivity.

is a rare genetic syndrome combining endocrine, skin, heart, and muscle-joint abnormalities.

is a rare condition combining gastrointestinal stromal tumors (GISTs), lung chondromas, paragangliomas.

is a rare inherited syndrome causing paragangliomas and gastrointestinal stromal tumors.

is a genetic disorder impairing fat use, causing fasting low blood sugar.

is a genetic muscle disorder causing exercise-triggered pain, weakness, and muscle breakdown.

is a severe inherited fatty-acid breakdown disorder in newborns, often life-threatening.

is a rare inherited disorder of fat breakdown causing life-threatening infant illness.

is an inherited problem processing fat, causing exercise-triggered muscle breakdown.

is a rare inherited fatty acid oxidation disorder causing life-threatening newborn crises.

is a rare metabolic disorder causing carnosine buildup and neurological problems.

is a rare inherited disorder causing enlarged bile ducts and infections.

is a rare inherited liver disorder causing bile duct dilation and scarring.

is harmless yellow-orange skin discoloration from excess dietary carotenoids, sparing eyes.

is narrowing of neck arteries (carotids) from plaque, raising stroke risk.

is a tear in the carotid artery wall causing stroke risk.

is a neck artery blockage reducing brain blood flow, raising stroke risk.