All diseases

OMIM ID
217700
OMIM term:
CORNEAL ENDOTHELIAL DYSTROPHY 2, AUTOSOMAL RECESSIVE; CHED2
Alternative terms:
CORNEAL DYSTROPHY, CONGENITAL HEREDITARY ENDOTHELIAL
CONGENITAL HEREDITARY ENDOTHELIAL DYSTROPHY OF CORNEA
MAUMENEE CORNEAL DYSTROPHY
(∗) Location:
20p13  
(†) Associated OMIM genes:
SLC4A11  
(‡) Associated MGI genes:

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