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 hemolytic anemia from oxidized hemoglobin (Heinz bodies) damaging red cells.
is a rare eye condition affecting the retina around the optic nerve.
is a serious pregnancy complication affecting the liver, blood, and blood pressure.
is a rare genetic condition affecting development, behavior, and learning.
is a usually noncancerous blood vessel tumor in brain or spinal cord.
is a noncancerous growth of blood vessels inside the abdomen.
is a usually harmless tangle of blood vessels in the liver.
is a rare benign lung blood vessel growth, sometimes causing breathing symptoms.
is a usually benign blood vessel growth behind or around the eye.
is a rare benign growth of blood vessels affecting a nerve.
is a usually noncancerous growth of blood vessels in the spleen.
is a noncancerous growth of blood vessels beneath the skin.
is a rare tumor that grows from blood vessel surrounding cells.
is a rare tumor that begins in cells around blood vessels.
is bleeding into a joint, causing pain, swelling, and stiffness.
is a blood-filled swelling around the testicle within its protective sac.
is a blood-related cancer affecting bone marrow, blood cells, or lymphatic system.
is a blood disorder linked to damage of peripheral nerves.
is a blood disorder that can also affect kidney function.
affects blood-forming tissues, disrupting blood cell production and immune function.
is a rare inherited disorder causing inflammation, anemia, and organ damage.
is a rare spinal birth defect affecting one side's nerves and tissues.
is a rare spinal birth defect affecting part of the spinal cord.
is a rare continuous one-sided headache disorder usually eased by indomethacin.