All diseases

OMIM ID
132000
OMIM term:
EPIDERMOLYSIS BULLOSA WITH CONGENITAL LOCALIZED ABSENCE OF SKIN AND DEFORMITY OF NAILS
Alternative terms:

(∗) Location:
3p21.31  
(†) Associated OMIM genes:
COL7A1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/z0icvu3t