All diseases

OMIM ID
122000
OMIM term:
CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 1; PPCD1
Alternative terms:
POSTERIOR POLYMORPHOUS CORNEAL DYSTROPHY; PPCD
CORNEAL DYSTROPHY, HEREDITARY POLYMORPHOUS POSTERIOR
(∗) Location:
20p11.21  
(†) Associated OMIM genes:
VSX1  
(‡) Associated MGI genes:
Dp(2Csrp2bp-6330439K17Rik)1Bra  

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* quick link - http://q.sanger.ac.uk/829b5m0d