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 bone disorder affecting growth, joints, and the spine.
is a rare genetic disorder affecting bone growth, joints, and stature.
is a genetic bone disorder causing short-trunk short stature and joint problems.
is a rare inherited disorder affecting bone growth, joints, and facial features.
is a rare inherited bone disorder causing short trunk and joint problems.
is a rare genetic skeletal disorder causing short stature and neonatal dislocations.
is a rare genetic bone disorder affecting the spine, joints, and feet.
is a rare genetic disorder affecting bone growth and the corneas.
is a rare genetic condition affecting bone growth, hand shape, and speech.
is a rare genetic syndrome affecting bones, skull, vision, and development.
is a rare genetic syndrome affecting bones, hearing, vision, and development.
is a rare genetic bone growth disorder affecting spine and joints.
is a rare genetic bone disorder affecting spine, joints, and growth.
is a rare genetic bone disorder affecting growth, spine, and joints.
is a rare inherited bone disorder causing short stature and joint problems.
is a rare genetic condition affecting bones, hearing, vision, and learning.
is a rare genetic disorder affecting bone growth, spine, and joints.
is forward slipping of a vertebra, often causing back and leg pain.
is a stress fracture in part of a spinal bone.
is a rare genetic bone disorder affecting the spine and growing bones.
is a rare genetic bone growth disorder affecting the spine and limbs.
is a rare genetic disorder affecting bones, spine, and corneas.
is a rare genetic bone disorder causing short stature and distinctive features.
is a rare genetic disorder affecting bone growth and vision.