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 inherited disorder causing skin, voice, and mouth changes.
is a common, harmless fatty lump that grows under the skin.
is a noncancerous fatty growth in the colon that may cause symptoms.
is a harmless fatty lump in the spermatic cord near the testicle.
is a condition causing multiple fatty lumps under the skin.
is a rare spinal birth defect where fatty tissue tethers the cord.
is a rare kidney disease causing protein leakage, swelling, and kidney failure.
is a rare cancer that starts in fat cells in soft tissues.
is a rare cancer that starts in the bone's fatty tissue.
is a rare ovarian cancer that starts in fatty tissue.
is a rare inherited disorder affecting energy production and early development.
is a rare inherited disorder that disrupts mitochondrial energy production.
is a rare inherited eye condition affecting the cornea's surface cells.
is a rare brain development disorder causing smooth brain surface and delays.
is a rare genetic brain-development disorder causing smooth cortex, delays, seizures.
is a rare genetic brain disorder causing smooth brain and severe delays.
is a rare genetic brain disorder causing a smooth brain and delays.
is a rare genetic brain development disorder causing a smooth brain.
is a rare genetic brain disorder affecting development, movement, and learning.
is a rare genetic brain development disorder causing smooth brain and delays.
is a rare genetic brain disorder causing smooth brain development problems.
is a rare tubulin gene brain disorder causing developmental delays and seizures.