All diseases

OMIM ID
204870
OMIM term:
CORNEAL DYSTROPHY, GELATINOUS DROP-LIKE; GDLD
Alternative terms:
CDGDL
AMYLOIDOSIS, CORNEAL
AMYLOID CORNEAL DYSTROPHY, JAPANESE TYPE
CORNEAL DYSTROPHY, LATTICE TYPE III
LATTICE CORNEAL DYSTROPHY, TYPE III
(∗) Location:
1p32.1  
(†) Associated OMIM genes:
TACSTD2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/4df55ny5