Typically the X-chromosome, which makes it more common in men.
The mutation can also occur on 19 other chromosomes, but X is the clearest one.
who discovered color blindness
color blindness night blindness snow blindness
Yes. See Wikipedia - Pingelap (#Color-blindness)
Individuals with color blindness often have a normal male karyotype (46,XY) or female karyotype (46,XX). The genetic basis for color blindness typically involves mutations in genes located on the X chromosome, leading to different types of color vision deficiencies.
female.
Color blindness is an example of an X-linked recessive trait, which is a type of non-Mendelian inheritance. This means that the gene responsible for color blindness is located on the X chromosome, and the trait is more commonly expressed in males than females.
It is not true that color blindness is most common in females. Color blindness is most common in males and approximately 8 percent of men have it.
The cause of color blindness is X-linked factors.
Color blindness is hereditary and non-communicable.
Colour (color) blindness is genetic and is not curable.-- The question asks whether red-green color blindness is treatable, not curable.
Colour (color) blindness is genetic and is not curable.-- The question asks whether red-green color blindness is treatable, not curable.
Color blindness is typically caused by mutations in genes located on the X chromosome. Males have one X and one Y chromosome (XY), so if they inherit the X chromosome with the color blindness gene, they will express the trait. In contrast, females have two X chromosomes (XX), so they would need to inherit the gene from both parents to exhibit color blindness, making it less common among females. This sex-linked inheritance pattern explains why color blindness is more prevalent in males than in females.