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 genetic disorder that impairs energy production in cells.
is a rare inherited disorder that impairs cellular energy production.
is an inherited mitochondrial disorder that affects energy production and body function.
is a rare genetic disorder that reduces cells' energy production.
is an inherited mitochondrial disorder that reduces the body's energy production.
is a rare genetic disorder that impairs cellular energy production.
is a rare genetic disorder that impairs cells' energy production.
is a genetic disorder impairing cellular energy, causing muscle and organ problems.
is a rare genetic disorder that reduces cells' ability to make energy.
is an inherited disorder that reduces cells’ ability to make energy.
is a rare inherited disorder that reduces cells’ ability to make energy.
is a rare inherited disorder that reduces cells' ability to make energy.
is a rare genetic disorder that disrupts cellular energy production.
is a rare genetic disorder affecting cellular energy production.
is an inherited disorder that lowers cellular energy and can affect organs.
is a rare inherited mitochondrial disorder that disrupts energy production.
is a rare inherited disorder that reduces cellular energy production.
is a rare inherited disorder that reduces the body's energy production.