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 skeletal disorder of growth plates, causing joint problems.
is a rare inherited bone disorder affecting joint development and growth.
is a genetic bone disorder affecting joint development, growth, and mobility.
is an inherited bone disorder causing joint pain, stiffness, and short stature.
is a genetic bone disorder affecting hip development, growth, and joint function.
is a rare congenital blockage of multiple intestinal segments causing bowel obstruction.
is a rare inherited bone disorder affecting growth near the joints.
is a rare genetic disorder that reduces cells' energy production.
is a rare inherited disorder affecting energy production and brain development.
is a rare genetic disorder that severely impairs the body's energy production.
is a rare inherited mitochondrial disorder affecting energy production and development.
is a rare inherited disorder that severely affects the body's energy production.
is a rare inherited disorder that affects energy production and development.
is a rare inherited disorder that disrupts the body's energy production.
is a rare genetic disorder that disrupts energy production and development.
is a rare inherited disorder that disrupts energy production and development.
is a rare inherited disorder that affects energy production and brain development.
is a condition causing nerve growths on the lips, tongue, and mouth.
is a cancer of bone marrow plasma cells causing bone, kidney problems.
is an inherited disorder causing multiple benign bone growths (exostoses), affecting joints.
causes multiple nerve-related tumors and too many red blood cells.
is a mental health condition with two or more distinct identities.
is a rare inherited disorder causing tumors in several hormone glands.
is a rare genetic disorder causing skin webbing and joint contractures.