is an inherited form of Alzheimer’s causing progressive memory and thinking decline.

is a genetic Alzheimer’s subtype causing progressive memory and thinking problems.

is a genetic form causing progressive memory, thinking, and daily function decline.

is an inherited Alzheimer’s subtype causing progressive memory, thinking, and behavior decline.

is a rare genetic disorder causing early blindness and excessive hair growth.

is reduced vision, usually one eye, from abnormal childhood visual development.

is a parasitic intestinal infection causing diarrhea, stomach pain, sometimes liver abscess.

is a rare genetic disorder affecting multiple body systems.

is a fast-growing skin cancer lacking pigment, often hard to spot.

is a rare condition where one or more entire limbs are absent.

is a congenital absence of one or both legs, affecting mobility.

is a birth defect with complete absence of one or both arms.

is a rare ectodermal disorder causing enamel defects, nail changes, reduced sweating.

is a rare, aggressive jaw cancer from tooth-forming tissue.

is a rare, benign jaw tumor with locally aggressive growth.

is a rare genetic syndrome with enamel defects, neurodevelopmental delays, hypohidrosis.

is an inherited enamel disorder causing weak, discolored, sensitive teeth.

is an inherited enamel disorder causing soft, discolored, easily chipped teeth.

is a genetic enamel disorder causing soft, discolored, and easily worn teeth.

is a genetic enamel defect causing soft, discolored, easily worn teeth.

is a genetic enamel formation disorder causing soft, discolored, fragile teeth.

is an inherited condition that causes abnormal tooth enamel formation.

is a genetic condition causing thin, weak tooth enamel and sensitivity.

is a hereditary enamel defect causing thin, fragile baby and adult teeth.