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 genetic disorder causing joint webs and anesthesia reactions.
is a lifelong immune condition affecting brain and spinal cord, disrupting nerves.
is a rare form of multiple sclerosis with somewhat different symptoms.
is a rare inherited condition affecting skin, nerves, and blood clotting.
is a rare inherited skin disorder causing recurring tumors that heal spontaneously.
is a usually slow-growing tumor affecting the tissues at the skull base.
involves multiple usually benign tumors around the spinal cord and canal.
is a rare inherited condition causing progressive brain, skin, and organ problems.
is a rare disorder causing symmetric noncancerous fatty growths around the neck.
is a rare genetic disorder causing progressive fusion of multiple joints.
is a rare genetic disorder causing progressive joint fusion and hearing loss.
is a rare genetic disorder causing joint fusions (synostoses) and hearing loss.
is a rare genetic condition causing joint fusions (synostoses) and hearing loss.
is a rare genetic disorder causing joint fusion and sometimes hearing loss.
is a rare neurodegenerative disorder affecting movement, balance, and automatic body functions.
is a rare brain disorder causing worsening balance, coordination, and autonomic problems.
is a rare brain disorder causing movement problems and autonomic failure.
is an inherited condition causing several congenital heart structure abnormalities.
is a rare, serious post-COVID illness causing widespread inflammation in children.
is a rare, serious inflammatory condition affecting multiple organs after infection.
is a rare inherited disorder affecting muscles, bones, and the brain.
is a rare genetic disorder affecting blood vessels, eyes, and other organs.
is a contagious viral illness causing swollen salivary glands and fever, vaccine-preventable.
is a form of abuse where a caregiver causes or fabricates illness.