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 an airway allergy from acid anhydride exposure, causing asthma-like symptoms.
is a rare inherited disorder causing harmful fat buildup in cells.
is a benign pituitary tumor causing hormone overproduction, often growth hormone.
is a rare pancreatic cancer from enzyme-producing acinar (exocrine) cells.
is a rare pancreatic cancer arising from enzyme-making acinar cells.
is a rare pancreatic cancer of acinar cells, often cystic.
is a healthcare-associated bacterial infection, often drug-resistant, affecting lungs, blood, wounds.
is a rare breast cancer that often grows slowly but can spread.
is a birth defect syndrome from prenatal acitretin or etretinate exposure.
is a common skin condition causing pimples, blackheads, and whiteheads.
is a rash with acne-like bumps, often triggered by medications.
is a noncancerous vestibular nerve tumor causing hearing loss, tinnitus, balance problems.
is nerve damage from amyloid buildup, causing numbness, tingling, weakness, autonomic problems.
is sudden bleeding around the brain from a ruptured aneurysm.
is a rare disorder causing sudden, recurrent swelling of skin, gut, airway.
causes recurrent airway or abdominal swelling from low C1 inhibitor, not inherited.
is characterized by recurrent swelling without hives from C1 inhibitor autoantibodies.
is an acquired immune disorder causing sudden swelling from low C1 inhibitor.
is coordination loss developing after birth from disease, injury, or toxins.
is reduced vasopressin (antidiuretic hormone) from pituitary-hypothalamic damage causing excessive urination, thirst.
is a long-term adrenal condition causing cortisol and aldosterone deficiency.
is loss of color vision (dyschromatopsia) from disease, injury, or medications.
is a rare, rapidly progressive prion brain disease from prion exposure.
is a rare disorder causing loose, sagging skin from elastic fiber loss.