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 sudden infection of ethmoid sinuses causing pain and swelling.
is sudden inflammation of the eustachian tube causing ear pain and fullness.
is a rare, life-threatening pregnancy complication causing sudden liver failure.
is acute infection of pelvic lining (peritoneum) causing severe lower abdominal pain.
is a rare spinal cord inflammation causing sudden limb weakness, mainly children.
is a sudden infection of the forehead sinus causing pain, congestion.
is a rare, sudden drug reaction causing widespread sterile pustules and fever.
is a sudden cervical infection from gonorrhea causing discharge, pain, and inflammation.
is a sudden gonorrhea-related bladder infection causing painful, frequent urination.
is a sudden uterine lining infection from gonorrhea causing pelvic pain, bleeding.
is a sudden sexually transmitted bacterial infection inflaming epididymis and testicles.
is a sudden prostate infection from gonorrhea, causing pain and urinary symptoms.
is a sudden gonorrhea infection inflaming fallopian tubes, causing pelvic pain.
is an immune reaction after transplant; donor immune cells attack the body.
is a contagious viral eye infection causing sudden redness and eye-surface bleeding.
is a rare, rapidly progressive brain inflammation with bleeding, requiring emergency care.
is sudden, severe pancreas inflammation with bleeding, requiring urgent emergency care.
is a rare genetic liver disorder causing sudden nerve and abdominal symptoms.
causes sudden corneal swelling, pain, blurred vision, and light sensitivity.
is a rare genetic mitochondrial disease causing infant liver failure.
is a rare genetic disorder causing infant liver failure, ataxia, and neuropathy.
is a rare genetic disorder causing infant liver failure and multisystem illness.
is a sudden outer ear infection, usually bacterial, causing pain, swelling.
is an acute heart attack affecting the heart’s lower and side walls.