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 cancer of the colon's connective tissues, requiring specialized treatment.
is a rare, aggressive colon cancer subtype with mucus-filled cells.
is a rare, fast-growing colon cancer that often spreads early and widely.
is a rare colon cancer arising from squamous (skin-like) cells.
is a birth defect blocking the colon in newborns, needing surgery.
is a noncancerous colon growth (polyp) that can sometimes become cancerous.
is a group of disorders affecting the colon, causing digestive symptoms.
is a rare colon neuroendocrine tumor producing glucagon-like peptide-1 (GLP-1).
is a rare, noncancerous lymphatic growth in the colon, often incidental.
is a condition mimicking bowel blockage without obstruction, causing bloating and pain.
is a brain disorder impairing color recognition despite normal color vision.
is an eye condition causing difficulty distinguishing certain colors, often inherited.
is spread by Rocky Mountain wood ticks, causing fever, headache, fatigue.
is a cancer starting in gland cells (adenocarcinoma) of colon or rectum.
is a noncancerous growth (polyp) in colon or rectum, potentially precancerous.
is a cancer of the colon or rectum, often treatable.
is a rare thyroid papillary cancer variant, often more aggressive.
is a trauma-related condition causing intrusive memories, hyperarousal, and avoidance after combat.
is a rare inherited bleeding disorder causing easy bruising and bleeding.
is a rare inherited bleeding disorder causing low factors VII and X.
is a rare inherited bleeding disorder causing low vitamin K–dependent clotting factors.
is a movement disorder combining dystonia with tremor, myoclonus, or parkinsonism.
is a rare, benign eye growth affecting retina and vision.