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 condition causing low levels of several pituitary hormones.
is a genetic condition causing hormone problems, hearing loss, and spinal abnormalities.
is a condition where the body makes too little growth hormone.
is a rare condition where the pituitary gland makes too few hormones.
is a condition present from birth causing low pituitary hormone levels.
is when the ovaries stop working normally before age 40.
is a buildup of fat in the liver not caused by alcohol.
is a rare kidney disease causing protein leakage and worsening kidney function.
is a rare disorder where abnormal antibodies build up in organs.
is sudden optic nerve damage causing painless vision loss, usually in one eye.
is a rare, aggressive cancer of primitive cells outside the brain.
is a rare inherited disorder affecting adrenal hormones and sometimes puberty.
is a fluid-filled sac in the kidney that develops later.
is a rare chromosomal disorder that can affect development and health.
is a rare chromosome disorder caused by missing genetic material on 12q.
is a rare chromosome condition caused by extra genetic material on 10q.
is a rare chromosome condition caused by extra material on chromosome 13.
is a rare chromosome condition caused by extra material on chromosome 9.
causes muscle weakness without the muscle breakdown seen in muscular dystrophy.
is an inherited condition causing thickened skin on the palms and soles.
is a rare genetic syndrome affecting teeth, upper jaw growth, and knees.
is a heart muscle disease that enlarges and weakens the heart.
is a heart muscle disease causing thickened walls and possible symptoms.
is a rare, noninherited condition causing an enlarged, weakened heart muscle.