- OMIM ID
-
121820
- OMIM term:
- CORNEAL DYSTROPHY, EPITHELIAL BASEMENT MEMBRANE; EBMD
- Alternative terms:
-
CORNEAL DYSTROPHY, ANTERIOR BASEMENT MEMBRANE
COGAN CORNEAL DYSTROPHY
CORNEAL DYSTROPHY, MAP-DOT-FINGERPRINT TYPE
CORNEAL DYSTROPHY, MICROCYSTIC
- (∗) Location:
- 5q31.1
- (†) Associated OMIM genes:
- TGFBI
- (‡) Associated MGI genes:
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