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 birth difference where one thigh bone is underdeveloped.
is a rare cancer that starts in the thighbone (femur).
is nerve damage in the thigh causing leg weakness, numbness, and pain.
is a blood clot and vein inflammation in the upper leg.
is a rare birth condition affecting the thigh bones and face.
is a rare birth condition affecting leg and arm bone development.
is a rare inherited skin condition causing recurring self-healing tumors.
is a rare genetic disorder affecting the brain, skin, and iron balance.
is an inherited iron overload disorder that can damage organs over time.
is a rare, usually benign tumor arising from fetal-type gland tissue.
is a rare disorder where low fetal movement causes deformities, often life-threatening.
is a genetic disorder causing reduced fetal movement and multiple birth defects.
is a rare genetic condition causing reduced fetal movement and birth differences.
is a rare genetic disorder causing reduced fetal movement and birth differences.
is a rare genetic disorder causing reduced fetal movement and birth defects.
is a rare inherited disorder causing reduced fetal movement and birth defects.
is a genetic disorder causing decreased fetal movement and brain, retinal bleeding.
is a group of lifelong problems caused by alcohol exposure before birth.
is a lifelong condition caused by alcohol exposure before birth.
is a rare pregnancy-related condition causing dangerously low platelet counts in newborns.
is a pattern of birth defects and developmental problems from anticonvulsant exposure.
is a rare birth defect pattern linked to carbamazepine exposure before birth.
is a congenital infection that can affect hearing, vision, growth, and development.
is a rare pregnancy condition where membranes can trap the developing baby.