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 parasitic infection caused by Guinea worms from contaminated water.
is inflammation around the heart that can develop after heart injury.
causes severe neck weakness, making it hard to hold the head up.
is an immune reaction (hypersensitivity) to medication, causing allergic symptoms.
is a condition where a person becomes unable to stop using drugs.
is lung scarring and inflammation caused by certain medicines or radiation.
is a temporary loss of reality caused by drugs or medication.
is a rare, serious drug reaction causing rash, fever, and organ damage.
causes high blood pressure in the lung arteries from drugs or toxins.
is a medicine reaction that makes your body destroy red blood cells.
is hearing damage caused by certain medicines, sometimes temporary but sometimes permanent.
is liver inflammation caused by medications, supplements, or other substances.
causes loss of fat tissue in one body area after medication use.
is a medication-triggered autoimmune condition that usually improves after stopping the drug.
is a mental health condition caused by the effects of drugs.
is inflammation of blood vessels triggered by certain medicines.
is a rare genetic kidney disorder causing severe problems before birth.
is a vitamin B1 deficiency that mainly damages nerves and muscles.
is a common condition causing dry, irritated eyes and blurry vision.
is a rare genetic disorder causing eye problems, muscle weakness, and scoliosis.
is a birth difference causing limited eye movement and eye retraction.
is a rare condition causing limited eye movement and congenital hearing loss.
is a rare inherited liver disorder causing lifelong mild jaundice (yellowing).
is a rare genetic condition affecting growth, development, and appearance.