ocular albinism 3

oc·u·lar al·bin·ism 3

(ok'yū-lăr al'bin-izm)
Visual disorder characterized by impaired vision, translucent irides, congenital nystagmus, photophobia, albinotic fundi with hyperplasia of the fovea, and strabismus; caused by mutation in the pinkeye gene (P) on 6q; autosomal recessive inheritance.