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 severe inherited disorder causing fragile bones, fractures, and short stature.
is a genetic disorder causing fragile bones, frequent fractures, and variable severity.
is a genetic disorder causing brittle bones and sometimes extra bone growth.
is a rare inherited bone disorder causing fragile bones, fractures, and deformity.
is a rare inherited bone disorder with fragile bones and short stature.
is a rare, severe inherited bone disorder causing frequent fractures from infancy.
is a rare inherited disorder causing fragile bones and frequent fractures.
is a rare inherited disorder affecting bones, teeth, and eye color.
is a genetic disorder causing fragile bones, eye problems, seizures, and delays.
is a rare genetic bone disorder affecting skull and skeletal growth.
is softening of the bones, usually caused by vitamin D deficiency.
is a rare inherited bone condition causing increased spine and pelvis density.
is a bone infection that causes pain, swelling, and fever.
is bone tissue death caused by reduced blood supply.
is an inherited condition where reduced blood supply causes bone tissue death.
is bone death in the jaw causing pain, swelling, and exposed bone.
is a rare genetic bone disorder affecting skull, bones, hearing, and development.
is a rare genetic condition affecting bones, skin, and hair pigment.
is an inherited disorder causing weak bones, intellectual disability, and sparse hair.
is a group of rare genetic disorders causing unusually dense, fragile bones.
is a rare genetic disorder causing dense bones and kidney acid problems.
is a rare inherited disorder causing unusually dense bones and weak immunity.
is a rare, usually harmless bone condition causing small, dense bone spots.
is a bone disease that weakens bones and increases fracture risk.