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 kidney disease causing progressive scarring and kidney failure.
is an inherited kidney disease causing scarring, cysts, and progressive failure.
is an inherited kidney disease that gradually leads to kidney failure.
is a rare genetic kidney disease causing scarring and early kidney failure.
is an inherited kidney disease that can lead to kidney failure.
is a rare inherited kidney disease that can lead to kidney failure.
is an inherited kidney disorder causing scarring, cysts, and early kidney failure.
is a rare inherited kidney disease causing childhood kidney scarring, cysts, failure.
is an inherited kidney disorder that gradually causes scarring and kidney failure.
is a rare inherited kidney disease causing scarring and early failure.
is a usually mild hantavirus infection that can affect the kidneys.
is kidney damage caused by an underlying storage or metabolic disorder.
is a rare genetic disorder affecting kidneys, hearing, and parathyroid glands.
is kidney damage caused by long-term high blood pressure and hardening vessels.
is a kidney disorder causing protein loss, swelling, and fluid buildup.
is a rare genetic syndrome affecting kidneys, hearing, urinary tract, and digits.
causes the kidneys to leak too much protein into urine.
is a rare inherited kidney disorder causing severe protein loss in urine.
is a rare inherited kidney disorder causing heavy protein loss in urine.
is an inherited kidney disorder causing severe protein loss in urine.
is a genetic kidney disorder causing severe protein loss in urine.