The correct option is B Phenylketonuria
Since, both a son and a daugther are affected in F1, the disorder is not sex-linked. So, it has to be autosomal. If the trait was dominant, then, the parents also would have been affected. Hence, the trait has to be controlled by a recessive gene. So, this pedigree is of autosomal recessive disorder, like phenylketonuria (PKU) and thalassemia.
Colour blindness and hemophilia are X-linked disorders.
Down's syndrome is chromosomal aneuploidy.