All diseases

OMIM ID
122200
OMIM term:
CORNEAL DYSTROPHY, LATTICE TYPE I; LCD1
Alternative terms:
LCD
LATTICE CORNEAL DYSTROPHY, TYPE I
CDL1
(∗) Location:
5q31.1  
(†) Associated OMIM genes:
TGFBI  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/u6t7142g