Autosomal recessive
Sexlinked and recessive.
Dimples are considered an autosomal trait, meaning they are inherited through genes located on autosomal chromosomes (non-sex chromosomes). This trait can be passed down from either parent to offspring regardless of gender.
Sickle cell anemia is a recessive genetic disorder caused by a mutation in the HBB gene, located on chromosome 11. It is inherited in an autosomal recessive pattern, meaning a person needs to inherit two abnormal copies of the gene (one from each parent) to have the disease. It is not an X-linked disorder or a multifactoial trait.
autosomal trait
sickle cell trait is inherited from one set of gene alleles from both parents. if you get two traits together it will cause sickle cell anemia which is a disease, sickle cell trait is not a disease. i dont know what autosomal means!! i dont know what codominance means!!
Nope! The disease is equally in both males and females. This means that it is autosomal.
Sickle cell anemia is an autosomal recessive disease. Carriers have sickle cell trait, which confers resistance to malaria.
Nope! The disease is equally in both males and females. This means that it is autosomal.
It is an autosomal recessive trait.
Sexlinked and recessive.
Sickle Cell Anemia is Autosomal Recessive. It arises from a mutation on the beta-globin gene of chromosome 11. Because Sickle Cell Anemia is an example of incomplete dominance, a person has the disease if they have two mutated beta-globin genes but only has the trait (is a carrier) if they have only one mutated beta-globin gene.
Alzaymrs is ottosomal dominent
Dimples are considered an autosomal trait, meaning they are inherited through genes located on autosomal chromosomes (non-sex chromosomes). This trait can be passed down from either parent to offspring regardless of gender.
Sickle cell disease is an autosomal recessive disorder, meaning that it is caused by a mutation in one of the autosomal chromosomes (chromosomes that are not sex chromosomes). In the case of sickle cell disease, the mutation occurs in the gene encoding the beta-globin subunit of hemoglobin on chromosome 11.
Albinism is a recessive, autosomal trait. So no, it is not sex-linked.
There is two answers, it is autosomal dominant showing incomplete dominace
Huntington's Disease is an Autosomal Dominant Trait, meaning that only one parent needs to pass the disease for the offspring to inherit it.