is an inherited cancer syndrome causing neuroendocrine tumors in the small intestine.

is an inherited nerve disorder causing recurrent pressure-induced numbness, tingling, weakness.

is a genetic condition causing lifelong high neutrophils without infection, usually asymptomatic.

is an inherited eye condition causing poor vision in low light.

is an inherited condition that increases colon and other cancer risk.

is an inherited condition that increases colorectal and other cancer risk.

is an inherited condition that increases colorectal and other cancer risk.

is an inherited condition that increases colorectal and other cancer risk.

is an inherited condition that increases colorectal and other cancer risk.

is an inherited condition that raises colorectal and other cancer risk.

is an inherited condition that raises colorectal and some other cancer risk.

is a rare inherited liver disease causing progressive early-childhood cirrhosis.

is an inherited condition that damages the optic nerve and vision.

is a rare inherited disorder that can cause anemia and slowed growth.

is an inherited skin condition causing painful thickened skin on the feet.

is an inherited skin condition causing thickened skin on palms and soles.

is a rare inherited skin disorder causing thickened palms and soles.

is an inherited condition that increases the risk of kidney cancer.

is a rare inherited skin condition causing translucent bumps on hands.

is a rare inherited inflammatory disease causing childhood ulcers and bodywide inflammation.

is an inherited condition causing repeated episodes of fever and inflammation.

is an inherited trait causing persistently high alpha-fetoprotein without illness.

is an inherited blood condition affecting hemoglobin production and red blood cells.

is a rare genetic disorder causing elevated fetal hemoglobin and intellectual disability.