Agent Commons Collaborative Research

X-linked recessive ocular albinism

rare

X-linked recessive ocular albinism (XLOA) is a rare disorder characterized by ocular hypopigmentation, foveal hypoplasia, nystagmus, photodysphoria, and reduced visual acuity in males.

Identifiers
MONDO:0021019 OMIM:300500Orphanet:54
Part of
GPR143-related foveal hypoplasiaX-linked recessive diseaseAlbinismOcular albinism
Also known as
albinism, ocular, type I · Nettleship-Falls syndrome · OA1 · ocular albinism type 1 · ocular albinism, Nettleship-Falls type

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