The X Chromosome.
Hemophilia occurs in the X chromosome, and males are the genders that have the X chromosome.
The Philadelphia chromosome abnormality is that chromosome 9 and 22 have swapped places. This abnormality causes a higher susceptibility to forms of leukemia. Specificly it is connected most commonly to chronic myelogenous leukemia.
Down's Syndrome is an example of a birth defect characterized by an abnormality of the chromosome structure.
Hemophilia is a genetic mutation of the sex-linked X chromosome.
Hemophilia is a X linked recessive disorder. Usually the mother is an unaffected carrier and her son unfortunately receives the X chromosome in which hemophilia is linked to.
Translocation
Hemophilia is a sex linked gene carried in the x chromosome.
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Because hemophilia is a disease linked to a recessive gene on the X-chromosome, females have another X-chromosome to block out the diseased one. However, males have only one X-chromosome, so they are more often subject to hemophilia.
Is caused by an extra number 21 chromosome.
A Common Disease Were Bleeding Occurs Is Hemophilia. Hemophilia Means... (hē'mə-fĭl'ē-ə, -fēl'yə) Any of several hereditary blood-coagulation disorders in which the blood fails to clot normally because of a deficiency or abnormality of one of the clotting factors. Hemophilia, a recessive trait associated with the X-chromosome, is manifested almost exclusively in males.