All diseases

OMIM ID
122100
OMIM term:
CORNEAL DYSTROPHY, MEESMANN; MECD
Alternative terms:
CORNEAL DYSTROPHY, MEESMANN EPITHELIAL
MEESMANN CORNEAL DYSTROPHY
CORNEAL DYSTROPHY, JUVENILE EPITHELIAL, OF MEESMANN
(∗) Location:
12q13.13   17q21.2  
(†) Associated OMIM genes:
KRT12   KRT3  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/9hdbf0u6