All diseases

OMIM ID
607541
OMIM term:
CORNEAL DYSTROPHY, AVELLINO TYPE; CDA
Alternative terms:
ACD
AVELLINO CORNEAL DYSTROPHY
COMBINED GRANULAR-LATTICE CORNEAL DYSTROPHY
GRANULAR CORNEAL DYSTROPHY, TYPE II; CGD2
(∗) Location:
5q31.1  
(†) Associated OMIM genes:
TGFBI  
(‡) Associated MGI genes:

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