All diseases

OMIM ID
133780
OMIM term:
EXUDATIVE VITREORETINOPATHY 1; EVR1
Alternative terms:
EXUDATIVE VITREORETINOPATHY, FAMILIAL, AUTOSOMAL DOMINANT
FEVR, AUTOSOMAL DOMINANT
CRISWICK-SCHEPENS SYNDROME RETINOPATHY OF PREMATURITY, INCLUDED; ROP, INCLUDED
(∗) Location:
11q14.2  
(†) Associated OMIM genes:
FZD4  
(‡) Associated MGI genes:
Fzd4  

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* quick link - http://q.sanger.ac.uk/tzcc08z1