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 medical emergency where a seizure lasts too long or repeats.
is a rare genetic condition causing skin cysts and natal teeth.
causes excess fat buildup in the liver, often without symptoms.
is a rare inherited condition affecting bones, joints, and growth from birth.
is an inherited disorder causing muscle weakness, stiffness, and other body-wide problems.
is blockage of the tear drainage system, causing watery or infected eyes.
is narrowing of the tear duct opening, often causing watery eyes.
is narrowing of the tear sac that can cause watery eyes.
is a childhood condition often causing repetitive, purposeless movements or self-injury.
is a rare inflammatory disorder causing bone pain, swelling, and skin pustules.
is a rare birth defect where the breastbone does not fully fuse.
is a rare cancer in the breastbone, often from nearby spread.
is a cancer of lymph cells affecting the breastbone (sternum).
is a rare genetic syndrome affecting steroid hormones and tooth development.
is an inherited condition that affects how the body makes steroid hormones.
is excess fatty tissue growth linked to long-term steroid use.
is high eye pressure caused by steroid medicines that can damage vision.
is an eye condition where steroid use raises pressure and damages vision.
is a rare autoimmune brain disorder that often improves with steroids.
is a rare genetic condition affecting cholesterol production and development.
is a rare inherited condition affecting how the body processes sterols.
is a rare inherited disorder affecting cholesterol processing and causing seizures.
is a rare, life-threatening reaction causing skin and mucous membrane peeling.
is a severe reaction causing blistering and skin loss across body surfaces.