Haemophilia is more commonly seen in human males than in human females because:

Explanation

Hemophilia is more commonly seen in males than females due to its inheritance pattern as an X-linked recessive disorder. Males have one X chromosome and one Y chromosome, so if they inherit an X chromosome carrying the mutation, they will exhibit the disease because they lack a second X chromosome to mask the effect of the mutation. Females, on the other hand, have two X chromosomes, so they would need to inherit two copies of the mutant allele to express the disease, making it less common among females. Option B accurately describes this inheritance pattern. Options A, C, and D are incorrect as they do not appropriately account for the genetic mechanism behind the prevalence of hemophilia in males.