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 genetic disease with fat buildup, enlarged liver, abnormal cholesterol.
is a nutrient deficiency causing liver and muscle damage, sometimes memory issues.
is a skin reaction causing small itchy hives from heat, exercise.
is a bone cancer subtype producing cartilage, causing pain and swelling.
is a rare benign bone tumor near joints, usually in adolescents.
is a group of rare skeletal disorders with stippled bone growth.
is a rare genetic bone disorder causing limb shortening and joint calcifications.
is a rare genetic skeletal disorder causing stippled bones and developmental differences.
is a rare inherited skeletal condition with joint dislocations and short stature.
is a rare genetic condition affecting bone growth and sex development.
is a genetic disorder affecting bones, ectodermal tissues, and night vision.
is a rare, slow-growing bone cancer near the skull base or spine.
is a rare, benign soft-tissue tumor causing a slow, painless lump.
is a rare, noncancerous (benign) sweat gland tumor of the vulva.
is a benign, slow-growing cartilage tumor in bone, often hands/feet.
is knee cartilage softening causing pain, swelling, and grinding with movement.
involves softening of kneecap cartilage, causing front knee pain and stiffness.
is a rare, noncancerous bone tumor, often in long bones.
is a cartilage cancer of bone that may spread.
is a rare, slow-growing brain tumor near the third ventricle, hypothalamus.
is a rare meningeal brain tumor, slow-growing but prone to recurrence.
is a rare cancer from notochord remnants along skull base and spine.
is a rare pregnancy-related movement disorder causing involuntary, dance-like movements.
is a pregnancy infection of the fetal membranes and amniotic fluid.