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.
causes early skull bone fusion and abnormal tooth development.
is a rare genetic condition causing skull, facial, brain, and developmental differences.
is a rare genetic syndrome causing skull, brain, and forearm abnormalities.
is a rare genetic disorder causing early skull fusion and brain calcifications.
causes early skull fusion, a small jaw, and severe developmental disability.
is a rare inherited skull disorder causing early skull bone fusion.
is a rare genetic condition causing early skull fusion and developmental differences.
is a rare inherited condition causing early skull bone fusion.
is a rare genetic condition affecting skull, facial, and brain development.
is a rare genetic disorder that affects bone growth and skull shape.
causes crater-like changes in the optic nerve that may affect vision.
is a group of genetic disorders reducing brain creatine, causing developmental delays.
is a rare inherited brain disorder that damages white matter.
is a skin infestation caused by fly larvae moving under skin.
causes rapid kidney inflammation that can quickly lead to kidney failure.
is a limited form of scleroderma affecting skin, blood vessels, and esophagus.
is a rare, progressive prion brain disease causing dementia and movement problems.
is a rare genetic condition causing developmental delays and a high-pitched cry.
is a rare, usually slow-growing cancer with a distinctive sieve-like pattern.
is a rare type of testicular cancer with a distinctive sieve-like pattern.
is a rare inherited disorder causing severe buildup of bilirubin.
is a rare inherited disorder causing severe, lifelong high bilirubin levels.
is a rare inherited liver disorder causing high bilirubin and jaundice.
is a serious tick-borne viral infection that can cause severe bleeding.