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Wilson disease is a rare inherited disorder. If both parents carry an abnormal gene for Wilson disease, there is a 25% chance in each pregnancy that the child will have the disorder.Wilson disease causes the body to take in and keep too much copper. The copper deposits in the liver, brain, kidneys, and eyes.auses. Wilson disease is a rare inherited disorder. If both parents carry an abnormal gene for Wilson disease, there is a 25% chance in each pregnancy that the child will have the disorder. Wilson disease causes the body to take in and keep too much copper.
Medical Definition of Wilson disease. Wilson disease: An inherited disorder of copper metabolism that results in an abnormal accumulation of copper in the body. Although the accumulation of copper begins at birth, symptoms of the disorder do not appear until later in life, between the ages of 6 and 40. A diagnostic feature of the disease is a Kayser-Fleischer ring, a deep copper-colored ring around the edge of the cornea that represents copper deposits in the eye.