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 blood clot in a brain vein that needs urgent care.
is a rare complication of kidney disease causing bone and facial changes.
is a rare inherited condition affecting development, hormones, and the nervous system.
is a rare inherited ciliopathy with bone, kidney, and eye problems.
is a rare inherited disorder causing severe bone, organ, and growth problems.
is a rare cancer that starts in the glands making saliva.
is a rare cancer that starts in the saliva-producing glands.
affects saliva-making glands, causing swelling, pain, dry mouth, or infection.
is a rare salivary gland cancer that affects mucus-producing gland cells.
is a salivary gland cancer that can range from slow-growing to aggressive.
is a rare breast cancer that resembles salivary gland tumors.
is a rare inherited disorder affecting brain development and movement.
is an infection usually causing diarrhea, fever, and stomach cramps.
is inflammation of the fallopian tubes, usually caused by infection.
is a condition where small pouches form in the fallopian tube wall.
is an infection and inflammation of the fallopian tubes and ovaries.
is a rare genetic syndrome with varied skin, growth, and developmental features.
is a rare genetic disorder causing inflammation and problems with blood cells.
is a rare genetic disorder affecting the nervous system and development.
is a rare inherited disorder that progressively damages the brain and nerves.
is a rare inherited disorder that gradually damages the brain and nerves.
is a rare inherited disorder causing rapid nerve damage in infancy.
is a rare inherited disorder causing progressive nerve cell damage in childhood.
is a rare condition causing unusual movements linked to acid reflux.