INHBA and Wilson disease: Similarly, a 19-gene combination, (EPR1, CREB3L1, BGN, CXCL10, UBE2S, INHBA, CEP55, BUB1, KIFC1, CDC45, SPATA17, CA12, CILP2, PTTG1, ADAMTS14, CLEC5A, FGD3, TNFRSF18, NEIL3), has been identified that could distinguish the MD group from the WD group with 94.2% classification accuracy (95.0% sensitivity and 92.2% specificity).