Home Page

References

OMIM

Gene

GeneReviews

HGMD

HGNC

GENATLAS PHENOTYPE

last update : 24-05-2014

Symbol	RP23
Location	Xp22.2
HGNC id	10277
Name	retinitis pigmentosa 23
Corresponding gene	OFD1
Main clinical features	characterized by constriction of the visual fields, night blindness, and fundus changes, including 'bone corpuscle' lumps of pigment
Genetic determination	sex linked
Function/system disorder	eye
Type	disease

Remark(s)