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 artery compression near the collarbone, reducing arm blood flow.
is a rare inherited connective tissue disorder causing twisted arteries and aneurysms.
is thickening of small arteries causing reduced blood flow and damage.
is hardening and thickening of arteries, reducing flexibility and blood flow.
is a peripheral artery disease causing narrowed leg arteries and poor circulation.
is plaque buildup in arteries, increasing heart attack and stroke risk.
is an abnormal tangle of blood vessels disrupting flow, risking bleeding.
is sudden vision loss from artery inflammation (giant cell arteritis).
is a condition where arteries narrow, reducing blood flow to tissues.
is joint inflammation causing pain, stiffness, and reduced movement; many types.
is a rare genetic connective tissue disorder with joint hypermobility and fragility.
is a group of conditions causing multiple joint contractures at birth.
is a genetic disorder causing multiple joint contractures present at birth.
is a genetic condition causing multiple joint contractures at birth, affecting movement.
is a genetic condition causing multiple congenital joint contractures and muscle weakness.
is a genetic condition causing multiple joint contractures present at birth.
is a rare genetic condition causing stiff joints (contractures) at birth.
is a rare genetic disorder with congenital joint contractures and facial tightness.
is a condition with multiple congenital joint contractures limiting movement.
causes congenital joint contractures and muscle weakness from spinal motor neuron loss.
is a rare genetic condition causing joint contractures (arthrogryposis) and ectodermal abnormalities.
is a genetic disorder with joint contractures and thickened skin; usually fatal.
is a rare genetic disorder causing hand contractures and sensorineural hearing loss.
is a rare genetic disorder causing joint contractures, eye-movement limits, retinal abnormalities.