All diseases

OMIM ID
604168
OMIM term:
CONGENITAL CATARACTS, FACIAL DYSMORPHISM, AND NEUROPATHY
Alternative terms:
CCFDN
CATARACT, CONGENITAL, WITH FACIAL DYSMORPHISM AND NEUROPATHY
(∗) Location:
18q23  
(†) Associated OMIM genes:
CTDP1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/hkplloi4