Hemophilia is a Sex-linked genetic disorder. It is found on the X chromosome of chromosome 23.
A carrier for Hemophilia(represented by H(dominant) or h(recessive)) would look like this:
XHXh(Female)
*Males are not carriers for hemophilia-They are either affected or they're not*
An affected person would look like this:
XhXh(Female) XhY(Male)
Someone who is neither a carrier nor affected would look like this:
XHXH(Female) XHY(Male)
Arthritis does not effect a chromosome.
No - the colour blindness gene is only found on the X chromosome.
without an X chromosome
Some are dominant ... some of the most noteworthy negative ones: color blindness, hemophilia are recessive.
the distance between genes on the same chromosome
26
The X Chromosome.
Hemophilia occurs in the X chromosome, and males are the genders that have the X chromosome.
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.
The "X" chromosome . . . I believe it is number 23 . . .
Hemophilia is a sex linked gene carried in the x chromosome.
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.
The X chromosome. That's why it's more common in males; females have 2 X chromosomes, but males only have 1. So if a woman has the hemophilia mutation on one of her chromosomes, she probably won't be affected by it.
It is carried on the X chromosome.
It is carried on the X chromosome.
Males only have one copy of the X chromosome