Could Malik have had hemophilia while lacking the blood clotting protein?

For someone to have hemophilia, which is a genetic disorder that affects the blood's ability to clot, they must have a defect in specific genes responsible for producing clotting proteins. If Malik is lacking the blood clotting protein necessary for normal clotting, it suggests that he has hemophilia, typically inherited as an X-linked recessive condition.

Understanding the nature of hemophilia is essential in unraveling the implications of inheritance. Hemophilia primarily affects males, as they have one X chromosome; if that X chromosome carries the gene mutation for hemophilia, they will express the condition. Females, with two X chromosomes, are often carriers if one X chromosome has the mutation, as they have a second X chromosome that can provide the normal copy of the gene.

If Malik is lacking the blood clotting protein completely, it would be entirely consistent with having hemophilia, indicating he could have inherited the disorder. Thus, the statement that he could not have inherited hemophilia contradicts the basic principles of genetic inheritance, particularly for an X-linked condition.

In summary, if Malik is missing the blood clotting protein, it directly correlates with the presence of hemophilia, affirming that he could indeed have inherited