Oculocutaneous albinism type 1
Oculocutaneous albinism type 1 is a genetic disease that affect coloring (pigmentation) of the skin, hair, and eyes. These conditions are caused by mutations in the TYR gene on chromosome 11.
OCA1
Oculocutaneous albinism type 1 is a genetic disease that affect coloring (pigmentation) of the skin, hair, and eyes. These conditions are caused by mutations in the TYR gene on chromosome 11.