Tel 6 motif characterized by the absence of both the KIR3DL1 and 2DS4 genes and the presence of the KIR3DS1 and 2DS1 genes was more frequent in CHC patients than in HCC (8.8% versus 1.7%, p = 0.02, Fig. 3B). The gene discussed is KIR3DL1; the disease is cryohydrocytosis.