Chromosome 21q22 which accounts for 20% of familial ALS.
Any chromosome can be affected by changes in chromosome numbers. This can include trisomy (three copies of a chromosome), monosomy (one copy of a chromosome), or other abnormalities such as deletions or duplications. These changes can lead to genetic disorders or abnormalities.
*affected
Lou Gehrig's disease, or amyotrophic lateral sclerosis (ALS), is primarily caused by mutations in the C9orf72, SOD1, FUS, and TARDBP genes. These mutations can lead to the degeneration of motor neurons in the brain and spinal cord. ALS is not specifically linked to a particular chromosome.
Meckel Syndrome (type 1)is an autosomal recessive trait carried on chromosome 17.
The allele that is responsible of Fabry Disorder/Disease is located on the X chromosome and is the only lipid storage disorder identified as being sex linked.
Chromosome 21q22 which accounts for 20% of familial ALS.
ALS is a disease of the neuromuscular system.
Chromosome 9.
Any chromosome can be affected by changes in chromosome numbers. This can include trisomy (three copies of a chromosome), monosomy (one copy of a chromosome), or other abnormalities such as deletions or duplications. These changes can lead to genetic disorders or abnormalities.
*affected
x
It's Chromosome X .
Lou Gehrig's disease, or amyotrophic lateral sclerosis (ALS), is primarily caused by mutations in the C9orf72, SOD1, FUS, and TARDBP genes. These mutations can lead to the degeneration of motor neurons in the brain and spinal cord. ALS is not specifically linked to a particular chromosome.
if you mean chromosome its the 15th......
13
Obviously.
Chromosome 21 is tripled in Down syndrome.