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 bacterial infection spread by ticks that causes fever and rash.
is an allergic reaction to quinidine that can be mild or severe.
is a rare scalp condition causing painful inflammation and permanent hair loss.
is a rare but serious viral infection that affects the nervous system.
is a rare genetic disorder causing severe insulin resistance and early diabetes.
is a rare condition causing underdeveloped forearm and lower leg bones.
is a rare birth difference with a partly or completely missing radius.
is a rare genetic condition affecting the arms, thumbs, genitals, and teeth.
is nerve damage that can cause wrist drop, numbness, and weakness.
causes weakness, numbness, or wrist drop from radial nerve damage.
is a rare genetic condition affecting arm development and nasal breathing.
is bladder inflammation and irritation caused by radiation therapy.
is a rare spinal cord injury caused by radiation treatment.
is inflammation and damage to the rectum after radiation therapy.
is a condition caused by damage from exposure to radiation.
is nerve damage caused by past radiation treatment to a nerve network.
is nerve root irritation causing pain, numbness, tingling, or weakness.
is a rare genetic condition affecting the forearms, kidneys, and sometimes hearing.
is a rare inherited disorder causing fused forearm bones and low platelets.
is a rare birth difference where both forearm bones are joined.
is a congenital fusion of two forearm bones in one arm.
is a rare birth difference where the forearm bones are joined.
is a rare genetic condition with forearm bone fusion and developmental delays.
is a rare condition causing forearm fusion, small head size, and scoliosis.