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 corneal infection, often affecting contact lens wearers.
is an immune reaction to amoxicillin causing hives, swelling, or breathing trouble.
involves harmful, nonmedical amphetamine use causing dependence, mental and physical harm.
is a rare cancer at the bile and pancreatic duct junction.
is a rare, aggressive cancer where bile and pancreatic ducts meet.
is a noncancerous tumor near bile and pancreatic ducts, sometimes blocking flow.
is a rare cancer where bile and pancreatic ducts meet the duodenum.
is a rare cancer where bile and pancreatic ducts meet the intestine.
is a rare cancer at the small intestine bile–pancreatic opening.
is a rare mucus-producing (mucinous) cancer at the bile-pancreatic junction.
is a rare, fast-growing neuroendocrine cancer where bile and pancreatic ducts meet.
is a rare cancer at bile and pancreatic duct opening causing jaundice.
is a rare cancer where bile and pancreatic ducts meet.
is a brain-based disorder causing trouble recognizing tunes and matching pitch.
is a rare, localized amyloid deposit forming a benign mass.
is a disorder where amyloid protein builds up, damaging organs and tissues.
is a rare skin disorder causing mottled light-and-dark patches due to amyloid.
is an autoimmune skin condition with typical rash, minimal muscle weakness.
is an inherited motor neuron disease causing progressive weakness and paralysis.
is a rare genetic motor neuron disease causing progressive weakness and paralysis.
is a rare inherited motor neuron disease causing progressive muscle weakness.
is a rare, inherited ALS subtype causing progressive weakness and paralysis.
is a progressive neurodegenerative disease of motor neurons causing weakness and paralysis.
is a rare, inherited motor neuron disease causing progressive muscle weakness.