All diseases

OMIM ID
120970
OMIM term:
CONE-ROD DYSTROPHY 2; CORD2
Alternative terms:
CONE-ROD DYSTROPHY; CORD
CONE-ROD RETINAL DYSTROPHY; CRD; CRD2
RETINAL CONE-ROD DYSTROPHY; RCRD2
(∗) Location:
19q13.33  
(†) Associated OMIM genes:
CRX  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/67tqeqwt