Medical

ocular albinism type 3

[MIM*203310]

type of ocular albinism 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.

Farlex Partner Medical Dictionary © Farlex 2012

Mentioned in

CLCN4
GPR143
ocular albinism 1
ocular albinism type 1
ocular albinism type 2
SHROOM2

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