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 inherited disorder affecting muscles, hearing, and energy production.
is a rare inherited disorder affecting digestion, nerves, muscles, and movement.
is an inherited condition causing hearing loss from mitochondrial gene changes.
is a genetic condition that reduces the body's ability to make energy.
is a genetic mitochondrial disorder that reduces the body's energy production.
is an inherited mitochondrial disorder that reduces cells' ability to make energy.
is a genetic disorder that reduces cells' ability to make energy.
is a group of inherited disorders that reduce the body's energy production.
is a rare inherited disorder affecting how cells make energy.
is a rare genetic disorder affecting how proteins enter mitochondria.
is a rare genetic disorder that disrupts energy production in cells.
is a rare genetic disorder affecting how mitochondria transport key molecules.
is a rare fat breakdown disorder causing energy crises and organ problems.
is a genetic disorder that impairs cells' energy production and function.
is a genetic mitochondrial disorder that can affect energy production and organs.
is a rare birth defect where the mitral valve never forms properly.
is a rare birth defect where the mitral heart valve is absent.
affects the heart valve between the left upper and lower chambers.
is a common heart valve condition where flaps bulge backward, sometimes leak.
is a narrowing of the heart's mitral valve that restricts blood flow.
is a rare brain or spinal cord tumor with mixed cell types.
is a rare brain tumor with features of several supportive brain cells.
is a rare immune disorder causing inflammation and autoimmune symptoms.
is a usually noncancerous gland tumor with more than one cell type.