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Disease Name: Leydig cell hypoplasia with pseudohermaphroditism
Genes Covered:AKR1C2, AR, CBX2, CYP11A1, DHCR7, DHH, DMRT1, HSD17B3, LHCGR, MAP3K1, NR0B1, NR5A1, SOX9, ZFPM2
Panel: Strand Clinical Exome Test
Disorder Category: 46 XY disorders
Turnaround Time: 5-6 weeks from receipt of sample in the lab