All diseases

OMIM ID
610651
OMIM term:
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP B; XPB
Alternative terms:
XP, GROUP B; XPBC XERODERMA PIGMENTOSUM B/COCKAYNE SYNDROME, INCLUDED
XPB/CS, INCLUDED
(∗) Location:
2q14.3  
(†) Associated OMIM genes:
ERCC3  
(‡) Associated MGI genes:
Ercc3  

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