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 fleas that causes fever and rash.
is a rare mosquito-borne viral brain infection that can become severe.
is a noncancerous muscle growth that usually does not spread.
is a genetic muscle disease causing weakness and sometimes heart problems.
is a group of conditions affecting muscles, causing weakness and pain.
is a rare genetic disorder affecting muscles, vision, and brain development.
is a rare genetic disorder affecting muscles, eyes, and brain development.
is muscle wasting that causes weakness and loss of muscle mass.
is a rare inherited disorder affecting muscles, balance, vision, and blood sugar.
is a group of inherited muscle disorders causing stiffness, weakness, or paralysis.
is a group of disorders that weaken muscles and affect movement.
is a group of inherited disorders that cause progressive muscle weakness.
is an inherited muscle disorder that causes progressive weakness and movement problems.
is a genetic muscle disease that causes weakness and developmental problems.
is a genetic muscle disorder causing weakness, developmental delays, and brain changes.
is a genetic muscle disorder causing weakness and brain or eye issues.
causes muscle weakness and brain and eye problems that vary widely.
is a rare inherited disorder causing muscle weakness and delayed development.
is a genetic disorder causing muscle weakness and sometimes brain involvement.
is an inherited muscle disorder that causes weakness and delayed development.
is a rare inherited muscle disease causing weakness and sometimes brain involvement.
is a rare inherited muscle disease that can also affect the brain.
is a genetic muscle disorder causing progressive weakness that varies by type.
is a group of inherited disorders that impair muscle energy use.