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 rare inherited disorder with polydactyly, genital blockage, and heart defects.
is a rare inherited disorder affecting the brain, nerves, blood, and muscles.
is a rare genetic disorder causing multiple severe birth defects.
is a highly contagious viral infection causing fever, rash, and cough.
is an outward-turning eyelid caused by scarring, swelling, or facial changes.
is a condition where the eyelid turns inward and irritates the eye.
is trouble fully closing the eyelids because something physically blocks closure.
is a rare inherited condition causing severe birth defects and organ malformations.
is a rare inherited disorder causing severe brain, kidney, and liver problems.
is a rare inherited disorder causing severe brain, kidney, and limb abnormalities.
is a rare inherited disorder causing severe birth defects, often life-limiting.
is a rare inherited disorder causing severe birth defects before birth.
is a rare inherited disorder affecting brain, kidneys, and other organs.
is inflammation of a small pouch in the intestine, causing belly pain.
is a small pouch in the intestine present from birth.
is a rare cancer arising in an extra pouch of intestine.
is a newborn breathing problem caused by inhaling meconium-stained amniotic fluid.
is a rare, benign bone condition causing pain near the collarbone.
is a rare condition where a ligament presses on an artery.
is a rare birth difference affecting the midline lip and lower jaw.
is a rare birth difference affecting the center upper lip and jaw.
is a rare birth difference affecting the center of the face.