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 inherited disorder causing a small head and developmental delay.
is a rare inherited condition causing a smaller-than-expected head size.
is a rare inherited condition causing a small head and brain changes.
is an inherited condition causing unusually small head size and developmental differences.
is an inherited condition causing a smaller head size and developmental differences.
is a rare inherited condition causing a small head and developmental delays.
is an inherited condition causing a very small head and developmental differences.
is an inherited condition causing an unusually small head and developmental delays.
is a rare genetic condition causing small head size and developmental differences.
is a rare inherited condition causing a very small head and delays.
is bone tissue death caused by reduced blood flow to a joint.
is an infection caused by bacteria that can affect many body parts.
is a condition where the upper spine pushes into the skull base.
is a chronic autoimmune liver disease damaging bile ducts, causing cholestasis.
is an inherited risk factor linked to autoimmune bile duct damage.
is an inherited liver disease causing bile duct damage and cholestasis.
is a rare inherited liver disease causing bile duct damage and scarring.
is an inherited liver disease that damages small bile ducts.
is a rare inherited liver disease causing progressive bile duct damage.
is a rare autoimmune liver overlap syndrome causing bile duct inflammation.
is a rare tuberculosis infection affecting bones, joints, and nearby tissues.
is a group of genetic disorders affecting bone and cartilage growth.
is a rare genetic bone disorder causing weak, underdeveloped bones.
is a rare genetic bone disorder causing soft, weak, poorly mineralized bones.