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 parasitic infection that mainly affects the urinary tract.
is a noncancerous growth in the urinary system.
is cancer that starts in the kidneys, bladder, or other urinary organs.
is a group of conditions affecting the kidneys, bladder, and urinary tract.
is a common infection affecting the bladder, urethra, or kidneys.
is a noninvasive bladder lining tumor that usually stays superficial.
is a blockage that slows or stops urine flow anywhere.
is a rare, noncancerous growth in the lining of the urinary tract.
is a rare metabolic disorder causing excess urocanic acid in urine.
is a birth defect affecting the urinary and reproductive organs.
is a tuberculosis infection affecting the kidneys, bladder, or reproductive organs.
is the formation of urinary tract stones causing pain and blockage.
is a skin reaction causing itchy hives from allergic or nonallergic triggers.
is a mast cell skin condition causing itchy brownish patches.
is a rare genetic disorder affecting facial features, heart, muscles, and bones.
is a genetic disorder causing hearing loss and progressive vision loss.
causes profound congenital deafness, balance problems, and early vision loss (retinitis pigmentosa).
is a genetic condition causing hearing loss, balance problems, and vision loss.
is a rare inherited disorder causing deafness, balance problems, and vision loss.
is an inherited condition causing deafness, balance problems, and progressive vision loss.
is a genetic condition causing early hearing loss, poor balance, worsening vision.
is a rare inherited condition causing deafness, balance problems, and vision loss.
is an inherited disorder causing deafness, balance problems, and progressive vision loss.
causes congenital deafness, balance problems, and later progressive vision loss.