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 malignant bladder tumor in the trigone causing urinary symptoms.
is a urinary tract infection from tuberculosis, causing painful, frequent urination.
is a rare bladder cancer subtype with tubulocystic (tube-and-cyst) clear cell features.
is a rare gland-forming cancer from urachal tissue near the bladder.
is a rare cancer from urachal (fetal duct) remnants near bladder.
is a rare, often aggressive cancer from urachal remnants near bladder dome.
is a rare cancer of the bladder lining (urothelial) from the urachus.
is a cancer of the bladder lining, often treatable when caught early.
is a bladder lining cancer with papillary (finger-like) growths, often noninvasive.
is a rare, slow-growing bladder cancer with wart-like growths, rarely spreads.
is a congenital fluid-filled brain cyst that sometimes causes hydrocephalus.
is a pediatric kidney cancer subtype characterized by predominant blastemal cells.
is a rare, aggressive blood cancer often presenting with skin lesions.
is a group of childhood cancers arising from immature cells (blasts).
is a fungal infection from inhaled spores, usually affecting lungs and skin.
is a rare inherited autoinflammatory disorder causing arthritis, rash, and uveitis.
is a bleeding disorder causing easy bruising from platelet collagen receptor defects.
is a rare platelet disorder causing easy bruising and prolonged bleeding.
causes easy bruising and mucosal bleeding from poor platelet adhesion.
is a rare bleeding tendency from poor thromboxane production affecting platelets.
is a rare inherited platelet disorder causing easy bruising and bleeding.
is a rare platelet function disorder causing easy bruising and bleeding.
causes bleeding symptoms from reduced factor VIII in some carriers.
is a tendency to bleed from reduced factor IX (FIX) activity.