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 collapsed lung that happens without injury or known lung disease.
is an early sexually transmitted infection that usually causes a painless sore.
is a spinal cord condition where a fluid-filled cavity forms.
is a rare disease where abnormal proteins build up in organs.
is a fungal infection that can spread through the body.
is a condition where spinal cord tissue is abnormally attached, causing symptoms.
causes low platelet counts, increasing easy bruising, bleeding, and petechiae.
is a rare inherited heart disease caused by abnormal fat buildup.
is a rare tuberculosis infection affecting the stomach or intestines.
is a tuberculosis infection of the lymph nodes, usually in the neck.
is a rare adrenal disorder causing hormone-related high blood pressure.
is a rare, aggressive cervical cancer made of immature nerve-like cells.
is a rare, aggressive uterine cancer from early nerve-like cells.
is a blood clot in the vein carrying blood to the liver.
is a type of chest pain caused by temporary coronary artery spasm.
is a rare, fatal brain disease caused by misfolded proteins.
is a rare inherited brain disorder causing progressive dementia and cell changes.
is a rare birth difference where a tube-like nose forms abnormally.
is inflammation of the rectum that can cause pain, bleeding, and urgency.
is a rare genetic condition causing early aging, short stature, and moles.
is a genetic disorder with premature aging, marfanoid build, and lipodystrophy.
is a rare genetic disorder linked to premature aging and liver cancer.
is a rare genetic disorder causing features of rapid aging.
is a rare genetic disorder causing rapid aging-like changes in childhood.