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 usually slow-growing cancer that starts in salivary glands.
is a rare esophageal cancer made of mucus-producing and squamous-type cells.
is a rare inherited disorder causing developmental, skeletal, and organ problems.
is a rare inherited disorder causing severe developmental, skeletal, and organ problems.
is a rare inherited lysosomal storage disease causing severe developmental delays.
is a rare genetic lysosomal disorder causing progressive skeletal and joint problems.
is a rare inherited disorder affecting bones, joints, and growth.
is a rare inherited lysosomal disorder affecting bones, joints, and growth.
is a rare genetic lysosomal disorder causing developmental delays and vision loss.
is a group of inherited disorders that affect metabolism and body tissues.
is a rare inherited condition causing sugar molecule buildup and organ damage.
is a rare inherited disorder causing harmful sugar buildup in cells.
is a rare inherited disorder impairing glycosaminoglycan (GAG) breakdown, causing skeletal abnormalities.
is a very rare inherited disorder affecting joints, soft tissues, and bones.
is a genetic condition affecting many organs (lysosomal storage disorder).
is a rare inherited disorder causing buildup of sugars that damages organs.
is a rare inherited disorder causing gradual buildup of sugars in cells.
is a rare inherited disorder causing progressive problems in many organs.
is a genetic storage disease (lysosomal storage disorder) causing progressive childhood neurodegeneration.
is a rare inherited disorder that affects bones, joints, and growth.
is a genetic disorder causing progressive skeletal problems from enzyme deficiency.
is a rare inherited disorder affecting bone growth and physical development.
is a rare inherited disorder causing buildup of sugars that harms organs.
is a rare inherited disorder causing harmful sugar buildup and fast worsening.