All diseases

OMIM ID
156600
OMIM term:
MICROCORIA, CONGENITAL
Alternative terms:
MCOR
MIOSIS, CONGENITAL
(∗) Location:
13q31-q32  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/g486eplr