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 syndrome causing spleen-gonad fusion, limb defects, and micrognathia.
is a rare birth defect where the spinal cord splits in two.
is a rare spinal birth defect where the spinal cord splits.
is a spinal birth defect where the spinal cord is split.
is a rare genetic condition causing limb differences and hearing loss.
is a rare genetic condition causing split feet and extra central fingers/toes.
is a rare genetic disorder causing short stature and bone abnormalities.
is inflammation of the spine that can cause pain and stiffness.
is a rare genetic bone disorder affecting growth, joints, and spine.
is a rare genetic disorder affecting the spine, bones, and eyes.
is a group of inflammatory joint diseases affecting the spine and joints.
is a rare genetic condition affecting bones, joints, and finger movement.
is a rare genetic disorder causing fused spinal, wrist, and ankle bones.
is a rare genetic condition causing abnormal spine and rib development.
is a rare genetic condition affecting spine and rib development.
is a rare genetic disorder causing abnormal spine and rib development.
is a rare genetic condition with malformed spine and ribs at birth.
is a rare genetic disorder affecting bone growth, spine, and joints.
is a rare inherited connective tissue disorder affecting bones, skin, and joints.
is a rare genetic disorder affecting bones, growth, and the immune system.
is a rare genetic bone disorder affecting the spine and joints.