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.
are birth defects of the aortic arch affecting blood flow.
is a rare congenital heart defect with a disconnected aortic arch.
is plaque buildup in the aorta, causing stiffness and cardiovascular complications.
involves the aorta (main artery), causing aneurysms, dissections, and rupture risk.
is a life-threatening tear in the aorta’s wall requiring emergency care.
is a structural aortic defect present at birth, altering blood flow.
is a rare aorta cancer that can block blood flow and spread.
is a heart valve problem causing narrowing or leakage, reducing blood flow.
is a disease of the aortic valve causing stenosis or regurgitation.
is a heart condition causing aortic valve narrowing (stenosis) or leakage.
is a genetic heart condition causing aortic valve narrowing or leakage.
is a heart valve disorder where blood leaks backward (regurgitation).
is a heart valve leaflet problem causing backward blood flow (aortic regurgitation).
is a narrowing of the aortic valve, limiting blood flow.
is inflammation of the aorta, from autoimmune or infections, risking aneurysms.
is a rare congenital heart defect creating an abnormal aorta–left ventricle connection.
is a rare congenital heart defect with aorta to right ventricle tunnel.
is a rare birth defect creating an abnormal aorta-to-ventricle connection.
is inherited APC gene condition with fewer colorectal polyps, increased cancer risk.
is a genetic condition causing early skull fusion (craniosynostosis) and webbed digits.
is a rare congenital disorder causing limb, spine, urinary, and intestinal malformations.
is a rare genetic disorder with missing digits, fused digits, microcephaly.
is a language disorder affecting speaking, understanding, reading, or writing.
is a rare genetic disorder affecting voice, hearing, vision, development, and feet.