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 condition causing an overactive thyroid in newborn babies.
is a urinary tract infection affecting newborn babies, usually caused by bacteria.
causes severe early-life inflammation affecting many organs, with very high IL-18.
is a rare inherited disorder causing liver problems in newborns.
is a serious eye disease caused by abnormal blood vessels raising pressure.
is inflammation of the kidneys that can affect how they work.
is a childhood kidney cancer (Wilms tumor), often curable with treatment.
is a condition where calcium builds up in the kidneys.
is a rare, usually noncancerous kidney tumor most often found in children.
is a rare, noncancerous growth in the bladder or urinary tract.
is a rare, usually benign growth in the urethra lining.
is a rare, noncancerous bladder growth often linked to irritation or injury.
is when kidneys resist antidiuretic hormone (ADH), causing excessive urination and thirst.
is a rare inherited kidney disorder causing excessive thirst and urination.
is a rare genetic disorder affecting kidneys, growth, brain, and facial development.
is a rare genetic disorder causing water retention and low blood sodium.
is a rare disease causing thickened skin in people with kidney failure.
is the formation of kidney stones causing severe side (flank) pain.
is a kidney tumor that may be benign or cancerous.
is an inherited kidney disease causing scarring and cysts, leading kidney failure.
is a genetic kidney disorder that often causes kidney failure in childhood.
is a rare inherited ciliopathy causing progressive kidney failure in childhood.
is a genetic kidney disease causing scarring, cysts, and early kidney failure.
is a rare inherited kidney disease causing progressive kidney failure in youth.