The distribution of RCDs was as follows: FVII deficiency(n = 53 [34%]), FV deficiency (n = 24 [15.4%]),FX deficiency (n = 23 [14.7%]), FXIII deficiency (n = 16[10.3%]), FI deficiency (n = 15 [9.6%]), FXI deficiency (n= 13 [8.3%]), FXII deficiency (n = 6 [3.8%]), plasminogendeficiency (n = 3 [1.9%]), and combined FV-VII deficiency(n = 3 [1.9%]). This evidence concerns the gene F5 and hyperinsulinemic hypoglycemia, familial, 4.