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, fast-growing cancer of placental cells, often after pregnancy.
is a rare, aggressive ovarian cancer producing pregnancy hormone (hCG), often chemotherapy-sensitive.
is a rare, aggressive brain cancer often causing bleeding and spread.
is a rare, aggressive testicular cancer that spreads early (metastasis).
is a healed scar of retina and choroid that can blur vision.
is inflammation of retina and choroid, usually infectious, impairing vision.
is a rare eye cancer arising in the choroid (uveal) layer.
is a disorder of the eye’s choroid, causing vision problems.
is a rare eye cancer of the choroid, often aggressive.
is a malignant choroidal eye cancer that impairs vision and may metastasize.
is a rare choroidal eye cancer that may cause vision loss.
is a rare brain tumor causing cerebrospinal fluid buildup and pressure.
is a rare, aggressive brain tumor from cerebrospinal fluid-producing tissue.
is a rare, usually benign brain tumor near cerebrospinal fluid pathways.
is a rare, usually benign brain tumor causing cerebrospinal fluid buildup.
is a rare brain tumor of cerebrospinal fluid–producing tissue, often in children.
is a choroidal eye cancer with spindle cells, affecting vision, potentially spreading.
is a rare genetic condition causing vision loss and early hair loss.
is an eye condition with choroid scarring, causing progressive vision changes.
is a rare inherited retinal disorder causing progressive vision loss, mainly males.
is inflammation of the eye’s choroid, often causing blurred vision.
is a rare X-linked genetic disorder causing developmental delays, seizures, ataxia.
is a skin allergy causing itchy, red rash after chromium exposure.
is a chronic fungal skin infection causing slow-growing warty lesions.