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 brain development condition with fluid buildup in the brain.
is a birth difference affecting brain development and balance, without excess fluid.
is a rare inherited bleeding disorder caused by platelet granule problems.
is a rare inherited skin condition causing thickened palms and soles.
causes an extra row of eyelashes that may irritate the eyes.
is a movement disorder causing involuntary muscle contractions and abnormal postures.
is an inherited eye condition where the lens shifts out of place.
means higher-than-normal muscle enzyme levels in the blood without other symptoms.
is a birth defect where brain tissue protrudes through a skull opening.
is a rare birth defect where the urethra opens abnormally.
is a rare neural tube defect with brain tissue outside the skull.
is a rare birth difference where the urinary opening is misplaced.
is a fatty growth in spinal tissue that may tether the cord.
is a brain development disorder that often causes seizures.
is a brain development difference that can cause hard-to-control seizures.
is a brain development difference that can cause seizures.
is a brain development difference that often causes hard-to-control seizures.
is a localized brain malformation causing seizures, often drug-resistant epilepsy.
is a brain malformation causing focal seizures and drug-resistant epilepsy.
is a brain development difference that can cause difficult-to-control seizures.
is a brain malformation that can cause hard-to-control seizures.
is a genetic skin disorder causing focal thickening on palms and soles.
causes thickened skin on the palms and soles, often inherited.
is a rare hormone disorder that reduces fertility and sexual development.