All diseases

OMIM ID
204000
OMIM term:
LEBER CONGENITAL AMAUROSIS 1; LCA1
Alternative terms:
AMAUROSIS CONGENITA OF LEBER I
LCA
RETINAL BLINDNESS, CONGENITAL; CRB
(∗) Location:
17p13.1  
(†) Associated OMIM genes:
GUCY2D  
(‡) Associated MGI genes:
Gucy2e   Gucy2f  

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* quick link - http://q.sanger.ac.uk/yx37204l