All diseases

OMIM ID
121900
OMIM term:
CORNEAL DYSTROPHY, GROENOUW TYPE I; CDGG1
Alternative terms:
GRANULAR CORNEAL DYSTROPHY, TYPE I; GCD1
CORNEAL DYSTROPHY, PUNCTATE OR NODULAR
(∗) Location:
5q31.1  
(†) Associated OMIM genes:
TGFBI  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/5trcv9vo