The explanation that describes why M are more likely to have linked disorders than W is that M have an X chromosome on which most linked disorders are located.
Linked inheritance refers to genes located on chromosomes that are involved in trait determination.
In humans, the male chromosome Y has few genes. On the other hand, the female chromosome X has a large number of genes involved in the determination of various characteristics.
XY chromosomes have small homologous regions at their ends. Thus, there is practically no recombination between their genes.
When the altered gene is on the X chromosome. This type of inheritance has a recessive pattern.
It is the maternal inheritance. In this case, sons inherit X chromosome genes only from their mother. Meanwhile, F daughters inherit one from the father and one from the mother.
The manifestations will be present because they have only one X chromosome, that is, they do not have any normal gene for that characteristic.
With this information, we can conclude that the manifestations will be present in men, as they have only one X chromosome.
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