is an inherited condition causing repeated pancreas inflammation and long-term damage.

is an inherited kidney cancer syndrome causing clear cell renal tumors.

is a rare inherited bleeding disorder affecting several vitamin K-dependent clotting proteins.

is a rare inherited nerve disorder causing ongoing muscle stiffness and twitching.

is an inherited kidney cancer syndrome that increases renal cell carcinoma risk.

is a genetic porphyria causing acute attacks and sometimes light-sensitive skin.

is an inherited red blood cell disorder causing dehydration and anemia.

is a rare inherited red blood cell disorder causing anemia and dehydration.

is an inherited tooth condition affecting dentin, causing weak, discolored teeth.

is an inherited condition that causes noncancerous but potentially aggressive tissue tumors.

is an inherited condition causing high risk of diffuse stomach cancer.

is a rare inherited white-matter (leukoencephalopathy) disease causing movement and thinking problems.

is an inherited red blood cell disorder causing oval-shaped cells and anemia.

is an inherited disorder causing brief episodes of poor balance and coordination.

is a rare inherited disorder affecting skin, muscles, joints, and lungs.

is a rare inherited disorder causing poor folate absorption, anemia, neurologic problems.

is an inherited disorder that makes the body unable to process fructose.

is a genetic disorder causing severe fructose intolerance and liver problems.

is an inherited condition that raises the risk of stomach cancer.

is a rare inherited disorder causing involuntary trembling of the chin.

is a rare inherited condition causing slow, noncancerous overgrowth of the gums.

causes fragile blood vessels, frequent nosebleeds, and abnormal connections (arteriovenous malformations).

is an inherited condition causing high carotene levels and vitamin A deficiency.

is a rare genetic disorder causing exaggerated startle and infant stiffness.