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.
involves genetic disorders affecting bone and cartilage growth, causing skeletal differences.
is a rare inherited condition affecting bone growth, hearing, and vision.
is a bone growth disorder affecting developing bones and nearby cartilage.
is an inherited disorder affecting bone and cartilage growth and development.
is a painful condition affecting blood supply to a metatarsal bone.
is a joint and bone condition affecting the foot's tarsal bones.
is a rare pancreatic tumor with unusual giant cells.
is a rare, severe genetic bone disorder affecting skull and limb development.
is a rare, noncancerous bone disorder that usually affects the shin.
is a genetic disorder causing fragile bones and frequent fractures, variably severe.
is the mildest form of brittle bone disease with frequent fractures.
is a rare inherited brittle bone disorder causing frequent fractures and deformities.
is a rare genetic disorder causing fragile bones and frequent fractures.
is a rare genetic disorder causing fragile bones and repeated fractures.
is a rare inherited disorder causing fragile bones and frequent fractures.
is a rare genetic bone disorder causing fragile bones and frequent fractures.
is a rare inherited disorder causing fragile bones and growth problems.
is a rare genetic bone disorder causing fragile bones and recurrent fractures.
is a rare genetic disorder that causes fragile bones and growth problems.
is a rare inherited brittle-bone disorder causing frequent fractures and bone weakness.
is a severe genetic disorder causing fragile bones before and after birth.
is a rare genetic disorder that causes fragile bones and fractures.