All diseases

OMIM ID
270300
OMIM term:
PEELING SKIN SYNDROME
Alternative terms:
PSS
PEELING SKIN SYNDROME, TYPE B
SKIN PEELING, FAMILIAL CONTINUOUS GENERALIZED
KERATOLYSIS EXFOLIATIVA CONGENITA
DECIDUOUS SKIN
(∗) Location:
6p21.33  
(†) Associated OMIM genes:
CDSN  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/bjoj2r98