X-linked disease
Fabry's disease has an X-linked, recessive pattern of inheritance, meaning that the defective gene is carried on the X chromosome.
CGD is an X-linked genetic disease, meaning the defective gene is carried on the X chromosome (one of the sex chromosomes). Females have two copies of the X chromosome, whereas males have one X and one Y.
Chromosome 4
No, Chromosome 4.
Gaucher's disease is located on chromosome 1, which is not the sex chromosome, so no. It is not a sex linked disease.
Chromosome 13
chromosome 17 The correct answer is chromosome 15
Huntington's disease is the result of a genetic defect on chromosome 4. This defect causes an excessive repetition of a section of the DNA on this chromosome. A unique characteristic of this disease is that as this gene gets passed down from generation to generation, the number of repeats of this DNA section increases. The more repeats that occur, the greater the chances of the carrier to develop symptoms of the disease at a younger age.
It's Chromosome X .
Sickle cell is a sex-linked trait, If some one is a carrier than the trait is passed down on that chromosome.
Kennedy's disease , an X-linked (carried by women and passed on to male offspring) SMA, features similar wasting of facial muscles as seen in ALS, with characteristic difficulty speaking and swallowing
Chromosome 16 has been a target of study by Crohns disease researchers lately and Chromosome 16 probably contains between 850 and 1,200 genes.