All diseases

OMIM ID
133540
OMIM term:
COCKAYNE SYNDROME, TYPE B; CSB
Alternative terms:

(∗) Location:
10q11.23  
(†) Associated OMIM genes:
ERCC6  
(‡) Associated MGI genes:
Ercc6   Xpa  

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* quick link - http://q.sanger.ac.uk/3sntkgjh