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 serious bacterial infection that inflames tissues around the brain.
is inflammation of the brain and surrounding tissues, usually from infection.
is a brain and blood vessel infection caused by untreated syphilis.
is a rare genetic condition causing developmental delays and distinctive facial features.
is a rare genetic disorder affecting copper levels, brain development, and growth.
is recurring fever linked to menstrual cycles, usually around menstruation.
is a rare inherited disorder affecting movement, learning, and nerve function.
is an allergic reaction to the local anesthetic mepivacaine.
is caused by toxic mercury exposure and can damage the brain.
is a rare, aggressive skin cancer that often grows quickly.
is an allergic reaction to the antibiotic meropenem, sometimes causing anaphylaxis.
is a rare inherited mitochondrial disorder causing seizures, muscle weakness, and fatigue.
is a rare inherited mitochondrial disorder causing seizures and muscle weakness.
is a kidney disease causing inflammation and blood or protein in urine.
is a tumor arising from connective tissue cells, benign or cancerous.
is a rare, aggressive cancer developing in bone or soft tissue.
is a rare tumor arising from connective tissue in the small intestine.
is a rare tumor made of several types of connective tissue.
is swollen lymph nodes in the abdomen, usually from an infection.
is a blocked blood vessel to the intestines, reducing blood flow.
is a seizure disorder from inner temporal brain scarring (hippocampus), often drug-resistant.
is a rare genetic condition causing fused digits and shortened finger bones.
is a congenital condition where the heart sits near the chest's center.
is a rare tapeworm infection that can affect the intestines or tissues.