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 chronic bile duct disease that causes inflammation and scarring.
is a rare, usually noncancerous lung tumor that often grows slowly.
is a rare liver cancer marked by scar-like tissue growth.
is corneal inflammation that causes scarring, clouding, and possible vision loss.
is a rare cancer that develops in fat tissue.
is a rare, usually benign tumor of the nerve sheath.
is a rare inherited disorder causing excessive bone growth.
is a sideways curvature of the spine that can vary in severity.
is a venomous sting that can cause pain and sometimes serious illness.
is a blind spot or area of reduced vision.
is a rare inherited bleeding disorder that affects normal blood clotting.
is a fatal prion disease affecting sheep and goats, not people.
is a parasitic infection caused by flesh-eating fly larvae in wounds.
is a usually harmless growth of blood vessels on the scrotum.
is a rare skin cancer that affects the scrotum.
is a rare skin cancer on the scrotum that usually grows slowly.
is a rare skin cancer that develops on the scrotal skin.
is an abnormal scrotal growth that may be benign or cancerous.
is a rare skin cancer affecting the scrotal skin.
is a rare skin cancer affecting the scrotum, usually in older adults.
is a bacterial infection spread by chigger bites, causing fever and rash.
is caused by severe vitamin C deficiency and can be treated.
is a rare disorder where certain cells build up fats.
is a type of depression linked to seasonal changes in daylight.