Yes,
the colour vision genes are apparently carried on the X of the XY pair of chromasomes (on the part that is missing anyway from the Y chromasome) and so can lead to a fairly simple genetic defect.
So, if a female is a carrier, one of her Xs is missing the important genetic material for colour vision and although she can have perfect colour vision from the other X chromasome, her sons have a fifty percent chance of inheriting the defect [added: and her daughter's a fifty percent chance of being carriers]. Of course, when there are only small numbers of offspring, it might miss them.
One of my two sons, my only brother and my mother's only brother are/were all affected, as is one of my older sister's two sons.
For a girl to be affected her mother must be a carrier and her father must be affected. In such a case, all the daughters will be carriers and fifty percent will again be likely to be affected.
There are however, two basic levels. One is red-green colour-blindness and the more severe is red-black. There may be other more rare defects too, that I am not aware of. In our family it's the more severe red-black colour-blindness. And it's not always the colours that you would expect that are confused. There seems to be absolutely no difference between blue and purple! I understand red-green affects about ten percent of boys overall and red-black only about one percent.