Hypopigmentation of the Skin is related to albinism, oculocutaneous, type ii and griscelli syndrome, and has symptoms including achromia of skin An important gene associated with Hypopigmentation of the Skin is TYR (Tyrosinase), and among its related pathways/superpathways is GPR143 in melanocytes and retinal pigment epithelium cells. Affiliated tissues include skin and myeloid, and related phenotype is pigmentation.