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 disorder causing birth defects, low muscle tone, seizures.
is a rare genetic disorder causing congenital anomalies, hypotonia, and seizures.
is a rare genetic disorder causing birth differences, hypotonia, and seizures.
involves multiple birth defects causing unusual physical features and health problems.
is a genetic condition causing multiple birth differences without intellectual disability.
is a rare genetic condition causing birth differences and intellectual disability.
is weakness or paralysis of several nerves controlling the head and face.
is an inherited disorder causing tumors in hormone-producing glands.
is an inherited disorder causing tumors in the thyroid and other glands.
is an inherited syndrome causing medullary thyroid cancer and endocrine tumors.
is a rare inherited syndrome causing endocrine tumors, especially medullary thyroid cancer.
is a rare inherited disorder causing tumors in hormone-producing glands.
is an inherited bone disorder affecting joint development, growth, and early arthritis.
is a genetic bone disorder causing joint pain and early arthritis.
is an inherited bone disorder affecting joint development, growth, and mobility.
is a genetic bone disorder affecting joint growth, pain, and mobility.
is a genetic bone growth disorder causing short stature and joint problems.
is a genetic bone disorder affecting joint development, growth, and movement.
is an inherited bone growth disorder affecting joints, height, and mobility.
is a genetic skeletal disorder causing joint pain, stiffness, and early arthritis.
is an inherited bone growth disorder affecting joints, height, and movement.
is a rare genetic bone disorder affecting joint development and growth.