is a rare birth foot deformity causing rigid rocker-bottom feet, affecting walking.

is a congenital condition causing rigid foot deformities in both feet.

is a rare foot condition present at birth, affecting one side.

is a rare genetic disorder affecting vitamin K-dependent clotting and causing bleeding.

is a genetic disorder at birth causing severe muscle weakness.

is a rare birth heart defect with reversed ventricles and arteries.

is a rare congenital ligament variant that may limit shoulder motion.

is a congenital heart defect with switched main arteries, reducing oxygen.

is a congenital heart defect with switched arteries and additional cardiac anomalies.

is a rare congenital heart defect causing misrouted blood and aortic narrowing.

is when the heart can't pump enough blood, causing fluid buildup.

is a rare fungal infection affecting nasal passages and facial tissues.

are rare identical twins born physically connected, sometimes sharing organs and tissues.

is difficulty moving both eyes together (gaze), usually from brainstem damage.

is a rare eye surface cancer affecting the conjunctiva’s tissues.

is a small calcified bump in eyelid lining, usually harmless.

is a benign eye surface change causing irritation, dryness, and redness.

is buildup of material on the eye’s lining (conjunctiva), causes vary.

is inflammation or disorders of the conjunctiva causing redness, irritation, discharge.

involves small lymphoid bumps on the eye surface from chronic irritation.

is a precancerous eye surface lesion that can become squamous cancer.

is a rare eye cancer on the conjunctiva that can spread.

is a common, harmless (benign) colored spot on the eye’s surface.

is dark discoloration of the eye’s conjunctiva, often benign melanin deposits.