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 serious lung injury caused by breathing toxic silo gas.
is a rare growth disorder causing poor growth before and after birth.
is a rare growth disorder affecting size, feeding, and development.
is a rare genetic growth disorder causing short stature and body asymmetry.
is a rare growth disorder causing poor growth and body asymmetry.
is a rare genetic condition causing poor growth before and after birth.
is a rare genetic growth disorder caused by two maternal chromosome 11 copies.
is a rare genetic growth disorder causing slow growth and body asymmetry.
is a rare genetic disorder causing intense hunger, obesity, and developmental differences.
is ongoing eye inflammation causing redness, irritation, and discharge.
is a condition where abnormal blood proteins can thicken in the cold.
is a seizure disorder causing brief focal seizures without loss of awareness.
is a group of abnormal blood vessel changes, often present at birth.
is a rare genetic overgrowth disorder causing distinctive features and developmental differences.
is a rare genetic disorder causing overgrowth and multiple birth defects.
is a rare brain-related condition causing difficulty seeing multiple objects at once.
is a genetic condition causing developmental delay, learning and speech difficulties.
is knee pain from overuse where the kneecap tendon attaches.
is a rare vasculitis affecting arteries in one organ.
is a rare genetic disorder affecting teeth, bones, and blood vessels.
is a heart rhythm disorder where the heart's natural pacemaker malfunctions.
is a rare inherited disorder causing slow heartbeat and congenital hearing loss.
is a rare, aggressive cancer that starts in the nasal cavity.
is inflammation of the sinuses, often causing congestion, facial pain, and pressure.