There was only genetic genotyping information for three patients: two with severe Factor VII deficiency (both homozygous for c.1109G > T pathogenic variant in FVII gene) and one with severe Factor XI deficiency (homozygous for the P.(CYS416TYR), c.1247 G > A missense mutation in exon 11 of the FXI gene). Here, F11 is linked to factor XI deficiency.