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 tumor of star-shaped brain cells (astrocytes) in children.
is a fast-growing blood cancer of B-lymphocytes in children, often curable.
is a rare childhood muscle cancer in mucosal areas, often treatable.
is a rare pediatric brain tumor, often curable with radiation-based therapy.
is a rare, usually benign tumor of the brain coverings in children.
is a rare pediatric brain tumor in the brainstem affecting vital functions.
is a tumor in the brainstem affecting vital functions in children.
is a brainstem tumor in children, affecting movement, balance, and cranial nerves.
is a fast-growing childhood cancer of the brain or spinal cord.
is a rare, highly treatable brain or spinal cord germ cell tumor.
is a rare, fast-growing germ cell tumor in brain or spinal cord.
is a rare, benign germ cell tumor in brain or spine.
is a rare childhood germ cell tumor of brain or spinal cord.
is a usually slow-growing cerebellar brain tumor in children, affecting coordination.
is a pediatric brain tumor in the cerebellum, causing coordination problems.
is a pediatric brain tumor of astrocytes, often slow-growing, treatable.
is a rare, aggressive ovarian cancer from placental cells, producing pregnancy hormone.
is a very rare, fast-growing childhood testicular cancer producing hormones.
is a rare childhood brain tumor from cerebrospinal fluid–producing tissue.
is a rare, aggressive central nervous system cancer in children.
is a rare, aggressive childhood cancer of the brain or spinal cord.
is a rare autism spectrum disorder with regression after normal early development.
is a rare autism spectrum disorder with regression after early development.
is an epilepsy syndrome with childhood-onset seizures and characteristic brainwave (EEG) patterns.