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 mitochondrial disorder that reduces cells’ energy production.
is a rare inherited mitochondrial disorder that reduces the body's energy production.
is a rare inherited mitochondrial disorder that impairs the body's energy production.
is a rare genetic disorder that impairs cellular energy production.
is a rare genetic mitochondrial disorder that impairs cellular energy production.
is an inherited mitochondrial disorder that affects energy production in cells.
is a rare inherited mitochondrial disorder that reduces cells' energy production.
is a rare inherited mitochondrial disorder that affects energy production and health.
is a rare inherited disorder that impairs energy production in cells.
is an inherited mitochondrial disorder that impairs cells' energy production.
is a rare inherited mitochondrial disorder that affects energy production.
is a nonfunctioning pituitary tumor that may affect vision and hormones.
is a very rare blood disorder with no Rh antigens.
is a rare leukemia with immature cells lacking B- or T-cell markers.
is an immune reaction to nuts that can sometimes be severe.
is a rare, aggressive cancer that often starts in midline body tissues.
is liver congestion usually caused by long-term right-sided heart failure.
is a health problem caused by too little or too much nutrition.
is caused by not getting enough essential nutrients for normal health.