All diseases

OMIM ID
121800
OMIM term:
CORNEAL DYSTROPHY, CRYSTALLINE, OF SCHNYDER
Alternative terms:
SCCD
SCHNYDER CRYSTALLINE CORNEAL DYSTROPHY
SCHNYDER CORNEAL DYSTROPHY; SCD
(∗) Location:
1p36.22  
(†) Associated OMIM genes:
UBIAD1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/f0typ79r