All diseases

OMIM ID
221900
OMIM term:
RETINAL NONATTACHMENT, NONSYNDROMIC CONGENITAL; RNANC
Alternative terms:
NCRNA
RETINAL DETACHMENT, CONGENITAL
(∗) Location:
10q21  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/d40zuo65