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 inflammation of the pituitary gland that can affect hormones and vision.
is a group of inherited disorders that weaken the immune system.
is a group of inherited disorders causing frequent, severe, recurrent infections.
is a rare inherited disorder that weakens the body's adaptive immune defenses.
is a rare immune disorder that weakens the body's first-line defenses.
is a rare inherited immune disorder that weakens the body's defenses.
is a rare inherited disorder causing recurrent infections and adrenal hormone deficiency.
is a rare inherited immune disorder causing severe illness after live vaccines.
is an inherited immune disorder causing unusually severe viral infections.
is a rare lung disease group affecting breathing in children and adults.
is a rare lung disorder affecting air sacs and causing breathing problems.
is a rare lung disease affecting air sacs and blood vessels.
is a group of adult-onset lung diseases that scar lung tissue.
is a rare childhood lung disease that can affect breathing.
is a rare childhood lung disease caused by abnormal air sac development.
is a rare childhood lung disease affecting air sacs and blood vessels.
is a rare childhood lung disease from surfactant gene changes.
is a rare bowel disorder causing protein loss from leaking lymph vessels.
is a rare brain tumor linked to changes in the DICER1 gene.
is a rare condition causing stones within the liver’s bile ducts.
is a rare, usually slow-growing tumor of lymphatic blood vessel cells.
is a rare eye cancer that starts in the eye's lymph tissue.
is a rare, usually benign blood vessel malformation inside bone.
is a rare tear gland disorder that can cause chronic dry eyes.