All diseases

OMIM ID
210370
OMIM term:
BIETTI CRYSTALLINE CORNEORETINAL DYSTROPHY
Alternative terms:
BCD
BIETTI TAPETORETINAL DEGENERATION WITH MARGINAL CORNEAL DYSTROPHY
(∗) Location:
4q35.2  
(†) Associated OMIM genes:
CYTOCHROME P450, FAMILY 4, SUBFAMILY V, POLYPEPTIDE 2  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/g0lpkeaz