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 birth defect causing shinbone bowing, fractures, and nonunion.
is a rare congenital condition causing ulnar nonunion (“false joint”) and deformity.
is drooping upper eyelid present at birth, sometimes affecting vision and development.
is a noncancerous lung development problem causing cysts and breathing issues.
is a rare, severe lung birth defect causing life-threatening newborn breathing problems.
is a lung birth defect causing large air-filled cysts.
is a congenital lung abnormality with multiple small cysts; severity varies.
is a rare congenital lung malformation affecting airway development before birth.
is a rare congenital lung malformation with large cysts, causing breathing issues.
is rare lung condition with enlarged lymph vessels causing newborn breathing trouble.
is a rare birth defect of lung tissue with abnormal blood supply.
is a congenital heart defect narrowing the pulmonary valve, reducing blood flow.
is a rare birth defect blocking lung veins, impairing oxygenated blood return.
is a birth defect where lung veins connect abnormally to the heart.
is a birth defect causing blocked pulmonary veins, straining heart and lungs.
is a birth defect affecting lung veins returning blood to heart.
is a birth condition where forearm bones fuse, limiting rotation.
is a congenital (present at birth) kidney artery narrowing raising blood pressure.
is a rare birth defect creating a bile–airway connection (fistula).
is an inherited skin disorder causing net-like scaling and redness from birth.
is a rare, present-from-birth abnormal artery-vein connection in the retina.
is from rubella infection in pregnancy, causing heart, eye, hearing defects.
is an inherited condition causing elevated red blood cells due to erythropoietin.
is a rare birth condition with too little small intestine, causing malabsorption.