The question seems to be incomplete, but based on the information given, if heterozygotes are unaffected, it suggests an autosomal recessive disorder.

Here's why:

1. In genetics, a heterozygote is an individual having two different alleles of a particular gene or genes, and so giving rise to varying offspring.

2. If a heterozygote is unaffected, it means they are a carrier of the disease but do not show symptoms. This is a characteristic of autosomal recessive disorders.

3. In an autosomal recessive disorder, two copies of an abnormal gene must be present in order for the disease or trait to develop. A person with an autosomal recessive disorder inherits one abnormal gene from each parent.

4. In contrast, in an autosomal dominant disorder, an affected person usually has one affected parent. A child of an affected parent has a 50% chance of inheriting the disorder. Therefore, if the disorder was autosomal dominant, a heterozygote would be affected.

So, based on the information given, the answer is an autosomal recessive disorder.

Question

The question seems to be incomplete, but based on the information given, if heterozygotes are unaffected, it suggests an autosomal recessive disorder.

Here's why:

1. In genetics, a heterozygote is an individual having two different alleles of a particular gene or genes, and so giving rise to varying offspring.

2. If a heterozygote is unaffected, it means they are a carrier of the disease but do not show symptoms. This is a characteristic of autosomal recessive disorders.

3. In an autosomal recessive disorder, two copies of an abnormal gene must be present in order for the disease or trait to develop. A person with an autosomal recessive disorder inherits one abnormal gene from each parent.

4. In contrast, in an autosomal dominant disorder, an affected person usually has one affected parent. A child of an affected parent has a 50% chance of inheriting the disorder. Therefore, if the disorder was autosomal dominant, a heterozygote would be affected.

So, based on the information given, the answer is an autosomal recessive disorder.

Knowee AI · Accepted Answer

The question seems to be incomplete, but based on the information given, if heterozygotes are unaffected, it suggests an autosomal recessive disorder.

Here's why:

1. In genetics, a heterozygote is an individual having two different alleles of a particular gene or genes, and so giving rise to varying offspring.

2. If a heterozygote is unaffected, it means they are a carrier of the disease but do not show symptoms. This is a characteristic of autosomal recessive disorders.

3. In an autosomal recessive disorder, two copies of an abnormal gene must be present in order for the disease or trait to develop. A person with an autosomal recessive disorder inherits one abnormal gene from each parent.

4. In contrast, in an autosomal dominant disorder, an affected person usually has one affected parent. A child of an affected parent has a 50% chance of inheriting the disorder. Therefore, if the disorder was autosomal dominant, a heterozygote would be affected.

So, based on the information given, the answer is an autosomal recessive disorder.

eterozygotes are unaffected.Group of answer choicesautosomal dominant disorderautosomal recessive disorderNext

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Heterozygotes are unaffected.

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