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Disease Name: Wilson disease
Genes Covered:HFE, ABCB6, ATP7A, ATP7B, CLDN16, CLDN19, CNNM2, CP, EGF, FTH1, FXYD2, HAMP, HFE2, KCNA1, SLC12A3, SLC30A10, SLC39A4, SLC40A1, TFR2, TRPM6
Panel: Strand Inborn Errors of Metabolism Test
Disorder Category: Disorders in the metabolism of trace elements and metals
Turnaround Time: 5-6 weeks from receipt of sample in the lab