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 bacterial infection from animals, often spread by unpasteurized dairy.
is a rare genetic disorder causing brittle bones and joint contractures.
is an inherited heart rhythm disorder raising sudden cardiac arrest risk.
is an inherited heart rhythm disorder increasing risk of sudden cardiac arrest.
is an inherited heart rhythm disorder causing life-threatening arrhythmias and fainting.
is an inherited heart rhythm disorder with arrhythmias and sudden cardiac arrest.
is an inherited heart rhythm disorder that can cause dangerous arrhythmias.
is an inherited heart rhythm disorder that raises sudden cardiac arrest risk.
is an inherited heart rhythm disorder causing life-threatening ventricular arrhythmias.
is an inherited arrhythmia disorder with abnormal ECG and sudden cardiac arrest.
is involuntary teeth grinding or clenching, often during sleep, causing wear.
is blockage of the liver (hepatic) veins causing pain and ascites.
is vessel inflammation linked to tobacco, reducing blood flow to limbs.
is a severe polio form affecting brainstem, causing breathing, swallowing problems.
is a rare urethral cancer in the bulbomembranous segment (mid-urethra).
is a genetic neuromuscular disease causing progressive weakness, speech and swallowing problems.
is an adult-onset genetic nerve disorder causing progressive limb and bulbar weakness.
is a rare, progressive nerve disorder causing weakness, swallowing and breathing problems.
is polio affecting brainstem and spinal nerves, causing paralysis and breathing problems.
is an eating disorder with bingeing, compensatory behaviors, and body-image distress.
is a rare infant skin disease with blisters from excess mast cells.
is a contagious staph skin infection with large, fragile blisters and crusts.
is corneal swelling (edema) causing painful blisters and blurred vision.