is an inherited condition causing reduced pigment in eyes, skin, and hair.

is an inherited condition causing low pigment in skin, hair, and eyes.

is a rare inherited condition causing reduced pigment in skin, hair, and eyes.

is an inherited condition causing reduced pigment and vision problems.

is an inherited condition affecting pigment, vision, and sometimes skin and hair.

is a rare genetic condition affecting eye development and teeth.

is a rare genetic disorder affecting the eyes, teeth, face, and fingers.

is a rare disorder affecting eyes, face, heart, and teeth, mostly females.

is a rare genetic disorder affecting the eyes, digestive system, and muscles.

is a rare genetic condition affecting vision, digestion, growth, and development.

is a rare bacterial infection causing red eyes and swollen lymph nodes.

is a sudden episode of uncontrolled upward eye movement and muscle spasms.

is a rare genetic disorder affecting the eyes, jaw, and face.

causes trouble moving the eyes on command, especially side to side.

causes eye movement problems, drooping eyelid, and sometimes double vision.

is a rare genetic condition affecting the eyes, bones, and skin.

is a rare genetic condition affecting the eyes, teeth, and ears.

is a genetic muscle disorder causing droopy eyelids and swallowing problems.

is a rare genetic muscle disease affecting the eyes, throat, and limbs.

is a rare inherited muscle disease affecting the eyes, throat, and limbs.

is a rare inherited muscle disorder affecting the eyes, throat, and limbs.

is a rare inherited muscle disease causing eye, throat, and limb weakness.

is a rare inherited muscle disease causing swallowing, eye, and limb weakness.

is a rare genetic disorder affecting the eyes, bones, and teeth.