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 rare genetic disorder causing joint contractures, kidney and liver problems.
causes congenital joint contractures and severe spinal curvature, affecting movement and breathing.
is a rare inherited disorder affecting joints, kidneys, and liver.
is a rare inherited disorder affecting joints, kidneys, and liver function.
is a joint disease causing pain, swelling, stiffness, and limited movement.
is a localized immune complex reaction causing painful, swollen injection-site inflammation.
is damage to joint cartilage causing pain, stiffness, and reduced mobility.
is a speech sound disorder affecting clear pronunciation and intelligibility.
is a rare genetic disorder causing brain malformations, seizures, and developmental delays.
is a rare genetic brain disorder causing early seizures and developmental disability.
is a throat (laryngeal) cancer affecting the aryepiglottic fold area.
is lung damage from inhaling asbestos fibers, causing scarring and cancer risk.
is a lung cancer caused by asbestos exposure; risk increases with smoking.
is a chronic lung disease from asbestos exposure causing scarring and breathlessness.
is an intestinal roundworm (Ascaris) infection, often mild but treatable.
is a roundworm intestinal infection causing abdominal symptoms and nutritional problems.
is an abnormality of the upper aorta, impacting structure and circulation.
is a serious bacterial bile duct infection from blockage; needs urgent treatment.
is cancer of the right colon, often causing hidden bleeding and anemia.
is a rare condition causing double lip, eyelid swelling, and goiter.
is nonbacterial meninges inflammation, usually viral, causing headache, fever, stiffness.
is uterine scar tissue (intrauterine adhesions) causing light periods, pain, and infertility.
is a rare, aggressive chest wall Ewing sarcoma in children and adolescents.
is an inherited lysosomal storage disorder causing progressive developmental and physical difficulties.