Ocular albinism type 1
id:
ocular-albinism-type-1-188-15862721
title:
Ocular albinism type 1
text:
Ocular albinism type 1 (OA1) is the most common type of ocular albinism, with a prevalence rate of 1:50,000. It is an inheritable classical Mendelian type X-linked recessive disorder wherein the retinal pigment epithelium lacks pigment while hair and skin appear normal. Since it is usually an X-linked disorder, it occurs mostly in males, while females are carriers unless they are homozygous. About 60 missense and nonsense mutations, insertions, and deletions have been identified in Oa1. Mutation
brand slug:
wiki
category slug:
encyclopedia
description:
Most common type of ocular albinism
original url:
https://en.wikipedia.org/wiki/Ocular_albinism_type_1
date created:
2008-10-22T22:59:51Z
date modified:
2024-09-09T00:39:04Z
main entity:
{"identifier":"Q2017756","url":"https://www.wikidata.org/entity/Q2017756"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/c/c7/X-linked_recessive.svg","width":600,"height":911}
fields total:
13
integrity:
16