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What is co-dominant disorder?

Updated: 12/7/2022
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Q: What is co-dominant disorder?
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Related questions

Why is sickle cell anemia a form of codominent inheritance?

To the best of my knowledge it is NOT codominant, but rather a simple autosomal recessive disorder. It may also be considered intermediate inheritance (a.k.a. incomplete dominance or overdominance) as heterozygotes are to an extent deficient in normal haemoglobin A production, only they usually do not show any clinical symptoms (and are protected from malaria as a bonus).


What trait is neither dominant or recessive?

Codominant.


Is breast cancer codominant or polygenic?

POLYGENIC!


Will A cross between two dominant homozygotes may produce a codominant animal.?

A cross between two dominant homozygotes may produce a codominant animal.


Do codominant alleles assort independently?

no the do not chromosomes assort independently


Is tay-sachs caused by codominant alleles?

No, autosomal recessive


What allele for the sickle cell trait is with the normal allele?

codominant


What is the allele for sickle cell trait with the normal allele?

codominant


Which are differences between dominant and codominant marker?

dominat mark are special primers which are required to amplify homozygous alleles while codominant markers are required to identify heterozygous nature of an individual.


Traits produced by two or more genes are codominant?

yes but the mans genes are shown more in the child is that your question cause i might be totaly wrong. ---- Genes from each parent show equally and codominant alleles produces a interleaved pattern rather than a blended pattern like incomplete dominance genes.


A person with the alleles ii has what blood type?

Which statement describes the blood type of a person with the alleles IAi? It is type AB because I and i are codominant. It is type AB because A and i are codominant. It is type A because i is dominant and A is recessive. It is type A because A is dominant and i is recessive.


Inheritance pattern of phenylketonuria and tay-sachs disease?

codominant alleles