All diseases

OMIM ID
135700
OMIM term:
FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 1; CFEOM1
Alternative terms:
OPHTHALMOPLEGIA, CONGENITAL
BLEPHAROPTOSIS WITH ABSENT EYE MOVEMENTS
FEOM1 LOCUS FIBROSIS OF EXTRAOCULAR MUSCLES, CONGENITAL, 3B, INCLUDED; CFEOM3B, INCLUDED
(∗) Location:
12q12  
(†) Associated OMIM genes:
KIF21A  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/akikpi2q