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 syndrome causing pelvic masses with abdominal and lung fluid.
is a rare bleeding disorder causing easy bruising and nosebleeds.
is a rare genetic bone disorder causing short stature and joint problems.
is a very rare genetic condition affecting growth, development, and appearance.
causes difficulty speaking, swallowing, and controlling facial movements from brain damage.
is a rare genetic disorder affecting bone growth and joint development.
is a rare type of testicular cancer with gland-like patterns.
is a difference in sex development affecting genitals or reproductive organs.
is a rare condition causing salt loss despite normal hormone signals.
is a rare inherited condition causing salt loss and high potassium.
is a rare inherited disorder causing high blood pressure and high potassium.
is an inherited kidney disorder causing high blood pressure and high potassium.
is a rare inherited disorder causing high potassium and high blood pressure.
is a genetic kidney condition causing high potassium, hypertension, and metabolic acidosis.
is an inherited condition causing high blood pressure and high potassium levels.
is a genetic kidney salt-handling disorder causing hypertension and high potassium (hyperkalemia).
is a rare inherited disorder causing resistance to parathyroid hormone.
is a rare inherited disorder causing hormone resistance and low calcium.
is genetic disorder causing parathyroid hormone resistance and low calcium, high phosphate.
is a rare genetic condition causing hormone resistance, low calcium, skeletal changes.
is a rare condition where the body resists parathyroid hormone.
is a rare inherited disorder causing hormone resistance and characteristic bone changes.
is a rare inherited disorder causing hormone resistance and low calcium levels.
is a rare genetic disorder causing severe insulin resistance and growth problems.