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 nail fold infection causing redness, swelling, and pain.
is a rare, usually slow-growing bone cancer on the bone surface.
affects the salivary glands near the ears, causing swelling or pain.
is a rare salivary gland cancer that often grows slowly but spreads.
is a rare salivary gland cancer that starts near the jaw.
is swelling of the parotid salivary glands, often causing pain and tenderness.
is a usually noncancerous fluid-filled cyst beside the ovary or fallopian tube.
is a rare autoimmune anemia causing red blood cell breakdown after cold.
is a movement disorder causing sudden episodes of involuntary movements.
is a movement disorder causing sudden episodes of involuntary muscle contractions.
is a rare movement disorder causing episodes of twisting, imbalance, and stiffness.
is a movement disorder causing brief involuntary movements triggered by exercise.
is a rare genetic disorder causing sudden, severe burning pain episodes.
is a rare headache disorder causing brief, severe one-sided head pain.
is a movement disorder causing brief involuntary movements triggered by sudden motion.
is a rare blood disorder causing red blood cell destruction and clots.
is a rare movement disorder causing sudden involuntary movements without movement triggers.
is an inflammatory eye condition affecting the area behind the iris.
is an allergy to parsley that can trigger itching, swelling, or hives.
is a skin allergy causing itchy rash after parthenolide contact.
is a blockage of blood flow to part of the retina.
is a congenital heart defect causing a hole between chambers.
is a congenital heart defect with abnormal valves and an underdeveloped ventricle.
is a congenital heart defect with a hole between the upper chambers.