All diseases

OMIM ID
121700
OMIM term:
CORNEAL ENDOTHELIAL DYSTROPHY 1, AUTOSOMAL DOMINANT; CHED1
Alternative terms:
CORNEAL DYSTROPHY, CONGENITAL HEREDITARY ENDOTHELIAL; CHED
CONGENITAL HEREDITARY ENDOTHELIAL DYSTROPHY OF CORNEA
MAUMENEE CORNEAL DYSTROPHY
(∗) Location:
20p11.2-q11.2  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/o76588ce