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.
includes body-wide diseases that can inflame the back of the eye.
is a rare, severe immune disorder linked to Epstein-Barr virus.
is a rare inflammatory disease with nerve damage affecting the whole body.
is a chronic autoimmune illness causing flares of widespread organ inflammation.
is a rare disease of mast cell buildup causing allergic-type reactions.
is a rare disease with abnormal mast cells and a blood cancer.
is a rare, potentially life-threatening poisoning that affects many organs.
is a fungal infection that can affect the lungs and other organs.
is a rare disease causing inflammation in medium-sized arteries throughout the body.
is a rare inherited disorder that impairs carnitine transport and energy production.
is an inherited condition impairing fat energy use (fatty acid oxidation).
is an autoimmune disease causing skin tightening and internal organ damage.
is a chronic autoimmune disease that causes skin and organ scarring.
is a group of blood vessel inflammations that can also damage kidneys.
is a childhood inflammatory disease causing arthritis, fevers, and bodywide symptoms.
is a condition where the heart cannot pump blood effectively.
is a rare immune disorder affecting T cells and natural killer cells.
is an immune disorder that weakens the body's ability to fight infections.
is a rare immune disorder causing severe vulnerability to infections.
is a rare genetic immune disorder causing life-threatening infections in infancy.
is a rare inherited immune disorder causing life-threatening infections early in life.
is a rare immune disorder causing absent T cells and severe infections.
is a rare inherited immune disorder causing life-threatening infections in infancy.
is an inherited immune disorder causing severe, early life-threatening infections.