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In your own sentences please

1. What is hemophilia?

2. Is hemophilia dominant or recessive?

3. What are the chromosomes for a female?

4. What are the chromosomes for a male?

5. Which chromosome is hemophilia attached/carried on?

6. Are males or females more likely to have hemophilia?

7. What is a carrier?

8. Who can be a carrier of hemophilia?

9. Does a carrier have hemophilia?

10. What are the alleles for a carrier of hemophilia?

11. What are the alleles for a male with hemophilia?

12. What are the alleles for a male with normal blood clotting?

13. What are the alleles for a female with normal blood clotting?

14. what are the alleles for a female with hemophilia?

15. What treatments are there for hemophilia? (may need to look this one up)

User Simcha
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1 Answer

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Answer: 1.Hemophilia is usually an inherited bleeding disorder in which the blood does not clot properly. This can lead to spontaneous bleeding as well as bleeding following injuries or surgery. Blood contains many proteins called clotting factors that can help to stop bleeding. 2.Hemophilia is a s3x-linked recessive disorder. The abnormal gene responsible for hemophilia is carried on the X chromosome. 3 and 4.chromosomes usually determine whether you are female or male. Women are XX. Men are XY. 4. 6.Although it is rarer for women to have hemophilia when compared to men, women can also have the condition. It is important to raise awareness about this fact to help women with hemophilia receive the care and support they need to live healthy lives. 7.A carrier, as related to genetics, is an individual who “carries” and can pass on to its offspring a genomic variant (allele) associated with a disease (or trait) that is inherited in an autosomal recessive or sex-linked manner, and who does not show symptoms of that disease (or features of that trait). thats all i know sorry!

Step-by-step explanation:

User Choonkeat
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