Below are statements that describe either traits that follow the typical pattern of mendelian inheritance or sex-linked inheritance patterns. sort them into the proper place

There are two types of the inheritance pattern observed in the humans.

1. autosomal inheritance,which follows the Mendelian Inheritance pattern.

2. Sex- linked inheritance.

The autosomal inherited condition are linked to the inheritance of the genes, which are present on the sutosomes not on the sex chromosome. they occur equally in both male and female progeny. Th inheritance is based on the type of allele inherited, whether it is dominant or the recessive one.

The sex linked disorders are those, which are linked to the sex chromosomes.  Most of the sex linked disorders occur due to the inheritance of the affected X chromosome. As the girls have two X chromosome, they are more likeley to be a carrier of the disease, hence, the sex linked traits occurs less in the female, as compared to the males.

The given table is the comparision of the sex linked inheritance and the autosomal inheritance.

The following statements Sex-linked traits:  

Hemophilia.

A trait like color-blindness, which affects many more men than women.

A trait that is linked to the X chromosome.

These are not equally likely to occur in males and females.

The following statements are Mendelian trait:

Involves a dominant and recessive allele.

A trait like eye color or height .

Predisposition to some diseases like diabetes and heart disease .

These are equally likely to occur in males and females.

Explanation:

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"1. it should be, it has been for about 20 years, and it's really not much different in the end than breeding animals to have particular traits. there are always concerns about genetically engineered animals/plants affecting the environment in unexpected negative ways, but i can't think of an example where the fears didn't turn out to be baseless.  

first, as you point out, it would be a great advance in pharmacology, to be able to tailor drugs and their doses to me. the pros involve better medical treatment. the cons involve privacy issues like insurance companies denying coverage to people with genetic risk factors. looking at dna markers wouldn't affect the frequency of genetic diseases, but it would allow detection of them earlier. and ok, actually i suppose that if people used this information to avoid having children with genetic diseases, some might decrease in frequency."