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 an aggressive brain cancer subtype affecting support cells and nerve-like pathways.
is an aggressive brain cancer subtype that often affects younger adults.
is a rare, usually benign fluid-filled cyst in the brain or spine.
is a rare brain or spinal cord tumor with mixed cell types.
is a rare, widespread brain tumor that affects multiple brain regions.
is a rare, aggressive brain tumor with both glial and sarcoma cells.
is a rare brain development disorder affecting balance, movement, and coordination.
is a rare genetic disorder with developmental delay, alopecia, and brain differences.
is a disorder causing developmental delay, lung cysts, overgrowth, and Wilms tumor.
causes delayed development, vision and nerve problems, seizures, and learning difficulties.
is a rare genetic disorder affecting development, bones, skin, hair, and teeth.
is a rare genetic condition causing delayed development, vision problems, and ataxia.
is a rare inherited disorder that damages the brain and nerves.
is a rare condition causing multiple painful growths from blood vessel cells.
is a rare, usually benign tumor arising from glomus body cells.
is a rare cancer arising from glomus cells around blood vessels.
is a group of kidney diseases that damage the kidneys' filtering units.
is a rare benign blood vessel growth often linked to POEMS syndrome.
is kidney inflammation of filters (glomeruli) causing blood, protein in urine.
is scarring of the kidney's tiny filters that can impair function.
is a usually benign growth that can cause severe localized pain.
is a rare inherited blood vessel disorder causing painful blue-purple skin lesions.
is inflammation of the tongue causing pain, swelling, and color changes.
is a rare condition where the tongue is fused to the palate.