All diseases

OMIM ID
278760
OMIM term:
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF
Alternative terms:
XP, GROUP F
XERODERMA PIGMENTOSUM VI; XP6
(∗) Location:
16p13.12  
(†) Associated OMIM genes:
ERCC4  
(‡) Associated MGI genes:
Ercc4  

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* quick link - http://q.sanger.ac.uk/foa6juhe