is a rare congenital lens defect causing notching and vision problems.

is a birth defect causing missing eyelid tissue and eye exposure.

is a congenital gap in the lower eyelid, affecting eye protection.

is a congenital gap in the iris, sometimes affecting vision.

is a birth defect with missing macular tissue, reducing central vision.

is a rare inherited condition affecting central vision and finger development.

is a birth defect of the optic nerve causing vision problems.

is a congenital defect of the optic nerve causing vision problems.

is a birth defect of the upper eyelid that risks corneal irritation.

is a rare genetic condition affecting eyes, bones, coloring, and hearing.

is a rare eye development disorder with coloboma, enlarged eyes, small corneas.

is a congenital eye disorder causing small eyes and ocular gaps (colobomas).

is a rare disorder causing eye defects, obesity, underdeveloped genitals, intellectual disability.

is a rare genetic disorder with coloboma and limb shortening (rhizomelia).

is a rare eye disorder causing congenital retinal defects and vision loss.

is a benign polyp that can turn into colorectal cancer over time.

is a cancer of the large intestine, usually arising from polyps.

is an early, noninvasive colon cancer (stage 0) confined to lining.

is a rare colon tumor linked to HHV-8 in weakened immunity.

is a rare, noncancerous (benign) smooth muscle tumor in the colon.

is a rare colon cancer from smooth muscle (leiomyosarcoma) cells.

is a rare cancer of lymphocytes arising in the colon.

is a colorectal cancer subtype with mucus-rich tumors starting in colon.

is a colon tumor of hormone-producing cells (neuroendocrine), behavior varies.