All diseases

OMIM ID
278780
OMIM term:
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP G; XPG
Alternative terms:
XP, GROUP G; XPGC
XERODERMA PIGMENTOSUM VII; XP7 XERODERMA PIGMENTOSUM, TYPE G/COCKAYNE SYNDROME, INCLUDED; XPG/CS, INCLUDED
CEREBROOCULOFACIOSKELETAL SYNDROME 3, INCLUDED; COFS3, INCLUDED
(∗) Location:
13q33.1  
(†) Associated OMIM genes:
ERCC5  
(‡) Associated MGI genes:
Ercc5  

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