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 eye misalignment where either eye turns inward alternately.
is a rare childhood neurological disorder causing recurrent one-sided paralysis episodes.
is a rare neurological disorder causing recurrent childhood episodes of one-sided paralysis.
is a rare tapeworm infection causing tumor-like liver damage and spread.
is inflammation of the tooth-supporting bone covering (periosteum), often painful.
is a fast-growing soft tissue cancer that can spread.
is a rare soft-tissue cancer, slow-growing yet prone to metastasis.
is a rare, benign lung tumor, usually found incidentally on imaging.
is a rare inherited amyloidosis from lysozyme protein buildup damaging organs.
is a rare, inherited form of Alzheimer’s causing early, progressive memory loss.
is a brain disorder causing progressive memory, thinking, and daily abilities decline.
is a hereditary form linked to gradual memory and thinking problems.
is a progressive brain disease causing memory loss and thinking problems.
is a progressive brain disorder causing memory loss and problems with thinking.
is a genetic form causing early-onset progressive memory and thinking decline.
is a genetic form of Alzheimer’s causing gradual memory and thinking problems.
is a progressive brain disease causing memory loss, confusion, and independence decline.
is a rare genetic Alzheimer’s subtype causing progressive memory and thinking decline.
is a rare inherited Alzheimer’s subtype causing early-onset progressive memory loss.
is a brain disorder causing progressive memory loss and thinking problems.
is a brain disorder that slowly destroys memory, thinking, and daily functioning.
is a rare inherited form causing early-onset memory loss and thinking problems.
is a rare inherited early-onset Alzheimer’s causing progressive memory and thinking decline.
is a rare autosomal dominant early-onset Alzheimer’s causing progressive dementia.