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Disease Name: Properdin deficiency, X-linked
Genes Covered:C1QA, C1QB, C1QC, C1R, C1S, C2, C3, C4B, C5, C6, C7, C8A, C8B, C9, CD59, CFB, CFD, CFH, CFHR5, CFI, CFP, COLEC11, CR2, FCN3, ITGB2, MASP2, SERPING1, THBD
Panel: Strand Clinical Exome Test
Disorder Category: Complement deficiencies
Turnaround Time: 5-6 weeks from receipt of sample in the lab