rs2032582 is a genetic variant on gene ABCB1 associated with Inflammatory bowel disease 13.
rs10876864 is a genetic variant on gene IKZF4 associated with Intelligence and Allergic disease.
rs11540652 is a genetic variant on gene TP53 associated with Li-fraumeni syndrome 1 and Multiple myeloma.
rs104894226 is a genetic variant on gene HRAS associated with Costello syndrome and Large congenital melanocytic nevus.
rs7274581 is a genetic variant associated with Alzheimer's disease.
rs10808546 is a genetic variant associated with Abdominal aortic aneurysm.
is a skin cancer subtype that can grow deeper than it appears.
is a rare, aggressive bladder cancer subtype that often spreads early.
causes harmless, tiny bumps on the lips or around the mouth.
is a rare condition where one or both eyes are abnormally small.
is a rare genetic condition affecting eye, brain, and finger development.
is a rare genetic disorder causing small eyes (microphthalmia) and limb differences.
is a rare genetic condition affecting eye development and the skin.
is a rare genetic condition with small eyes, fused eyelids, and delays.
is a spectrum of eye malformations causing small/absent eyes, coloboma, vision loss.
is a rare genetic condition affecting eye development and brain growth.
is a genetic syndrome causing small eyes, ear changes, and fetal immobility.
is a rare inherited eye disorder causing progressive vision problems.
is a rare genetic condition causing unusually small eyes and vision problems.
is a small, usually benign breast growth inside a milk duct.
is inflammation of the colon causing chronic, watery diarrhea without bleeding.
is a rare autoimmune disease causing inflammation of small blood vessels.
is a rare genetic condition affecting the eye lenses and bones.
is an infection caused by tiny parasites, often affecting the intestines.
is a birth difference where one or both outer ears are underdeveloped.
is a rare genetic condition affecting ear, eye, and tear duct development.
is a very rare chromosome change with features that vary widely.
is a rare genetic gut disorder causing severe newborn diarrhea and dehydration.
is a rare reflex seizure condition triggered by urination.
is a rare skin disorder causing fine wrinkling from lost elastic fibers.