- Wilson disease is a disorder that prevents your body from getting rid of extra copper. Too much copper ... Wilson disease is a rare inherited disorder that prevents your body from getting rid of extra copper. You ...
- Wilson's disease; Hepatolenticular degeneration ... Wilson disease is a rare inherited disorder. If both parents carry a defective gene for Wilson disease, there ...
- ... established. Learn more about the genes associated with Wilson disease ATP7B PRNP Inheritance This condition is inherited in ...
- Penicillamine is used to treat Wilson's disease (an inherited condition that causes copper to build up in the body and may result in serious symptoms) and cystinuria (an ...
- Diabetic nephropathy; Nephropathy - diabetic; Diabetic glomerulosclerosis; Kimmelstiel-Wilson disease
- ... waste products. Health Conditions Related to Genetic Changes Wilson disease Researchers have identified more than 250 ATP7B gene mutations that cause Wilson disease. About half the mutations change one of the ...
- ... signs and symptoms. More About This Health Condition Wilson disease The Met129Val polymorphism has been reported to influence the onset of Wilson disease, an inherited disorder in which excessive amounts of ...
- ... often used with other tests to help diagnose Wilson disease . Wilson disease is a rare genetic disorder that prevents the body from removing extra copper. Wilson disease can lead to a harmful buildup of copper ...
- ... group >Problemas del metabolismo</group><language-mapped-topic >Wilson Disease</language-mapped-topic><primary-institute >Instituto Nacional de ...
- ... published></health-condition-summary><health-condition-summary ><name >Wilson disease</name><ghr-page >https://medlineplus.gov/genetics/condition/ ...
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