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, usually noncancerous fatty tumor in the kidney.
is a rare cancer of fatty tissue affecting the kidney area.
is an extremely rare kidney cancer that forms bone-like tissue.
is damage to kidney papillae that can cause pain and bloody urine.
is a rare cancer that starts in the kidney's urine-collecting area.
is a rare aggressive cancer of the kidney pelvis lining.
is a rare, aggressive kidney cancer usually affecting infants and young children.
is a rare cancer that starts in the kidney's connective tissues.
is a rare genetic condition affecting kidney tubules and weakening heart muscle.
is when a wrist bone loses blood supply and can collapse.
is a rare inflammatory condition causing swollen lymph nodes and fever.
is a rare inflammatory disease causing painless head and neck lumps.
is a rare inherited skin disorder causing blistering, fragility, and sun sensitivity.
is a rare genetic disorder linked to muscle weakness and malignant hyperthermia.
is a rare genetic condition that can affect development and health.
is a rare bile duct cancer that starts where ducts join.
is a rare bile duct cancer occurring where the ducts join.
is a bacterium that can cause serious infections, especially in hospitals.
is a genetic condition causing developmental delay, intellectual disability, and congenital anomalies.
is a rare genetic condition causing developmental delay and distinctive features.
is a rare genetic condition affecting development, learning, behavior, and muscle tone.
is a rare disorder causing repeated extreme sleepiness and behavior changes.
is a genetic condition causing developmental delays, feeding difficulties, and sweating problems.