A 5-year-old boy was just diagnosed with red green color blindness. His parents are concerned and want clarification regarding how their son got this disorder

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A 5-year-old boy was just diagnosed with red–green color blindness. His parents are concerned and want clarification regarding how their son got this disorder because they have a daughter who does not have the disorder. Answer the following questions his parents have about the new diagnosis. 1.In what manner is red–green color blindness inherited? (e.g., monogenic, multifactorial, autosomal, X linked). Briefly describe monogenic vs multifactorial and autosomal vs. X linked Red-green color blindness is a type of X-linked recessive genetic inheritance and this gene can be found on the sex chromosomes. Dlugasch and Story (2023) posits that males possess a single X and Y chromosome, while females have two X-chromosomes. In addition, X-linked recessive disorders include red-green color blindness, and affect males and females differently. Males only have one X-chromosome, so if they possess the gene coding for red-green color blindness, they will express it and if they don’t have the gene, they will not express it. Females have 2 X-chromosomes, so even if she carries this undesired gene on one of her X-chromosomes, she is still protected by her second healthy chromosome. This is why females would require a copy of this gene on both x-chromosome to express it; only having one copy categorizes females as carriers and in this case they don’t express it. To provide more understanding about types of inheritance, monogenic inheritance is the inheritance of a trait determined by one gene. Monogenic inheritance is illustrated by red-green color blindness, due to mutations in a single gene, namely, OPN1LW or OPN1MW, both located on the X-chromosome (Dlugasch

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