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
Gaucher's disease is located on chromosome 1, which is not the sex chromosome, so no. It is not a sex linked disease.
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.
No, Parkinson's disease is not caused by a mutation on chromosome 6. The exact cause of Parkinson's disease is not fully understood, but it is believed to involve a combination of genetic and environmental factors. Some rare forms of Parkinson's disease are linked to specific gene mutations, but these are not located on chromosome 6.
It's Chromosome X .
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.
Chromosome numbers: 1, 14, 19, and 21 are affected by Alzheimer's disease.
Sickle cell disease is caused by a mutation on chromosome 11, specifically in the HBB gene that codes for the beta-globin protein. This mutation leads to the production of abnormal hemoglobin, resulting in the characteristic sickle-shaped red blood cells.
for son x chromosome comes from mother and y chromosome from father. If the mother had both allele got affected then the transfer of disease is 100 %. If only one allele is affected then 50% possibility of son getting affected