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The information on this page is for informational purposes only and does not constitute medical advice. Consult your genetic counselor or specialist physician for treatment decisions.
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Wilson Disease
Wilson Disease
Prevalence:
1/30000
hepatic
Official
·
OMIM:277900
Official
·
ORPHA905
Copper metabolism disorder and hepatolenticular degeneration due to ATP7B gene mutations.
Associated Genes
ATP7B
ATPase Copper Transporting Beta
Chromosome 13
Autosomal Recessive