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 serious eye infection with pus inside the eye.
is when the gel inside the eye pulls away from the retina.
affects the clear gel inside the eye and may blur vision.
is a common age-related change where the eye's gel becomes thinner.
is a rare genetic muscle disorder causing voice, swallowing, and limb weakness.
is a rare autoimmune disease affecting the eyes, skin, ears, and brain.
is a hand and forearm deformity caused by muscle damage.
is a rare brain inflammation causing extreme sleepiness and movement problems.
is an inherited disorder causing benign and cancerous tumors across organs.
is a very rare genetic syndrome with limited published medical information.
is a common inherited bleeding disorder causing easy bruising and prolonged bleeding.
is a common inherited bleeding disorder causing easy bruising and nosebleeds.
is an inherited bleeding disorder with defective von Willebrand factor function.
is an inherited bleeding disorder causing easy bruising and frequent nosebleeds.
is an inherited bleeding disorder causing poor platelet sticking and easy bleeding.
is an inherited bleeding disorder that reduces factor VIII clotting support.
is a severe inherited bleeding disorder from absent von Willebrand factor.
is a bleeding disorder caused by problems with blood clotting protein.
is a common inherited bleeding disorder from low von Willebrand factor.
involves sexual arousal from watching unsuspecting people who are naked or intimate.
is a rare inherited brain disorder that affects myelin and development.
is a rare genetic condition affecting development, learning, behavior, and sometimes seizures.
is a rare cancer that starts in gland cells of the vulva.