has material basis in germline mutation in CDSN generalized peeling skin syndrome peeling skin syndrome peeling skin syndrome 1 MEDGEN:1885521 peeling skin syndrome caused by mutation in CDSN GARD:0017259 generalized deciduous skin type B DOID:0070520 inflammatory peeling skin syndrome skin peeling, familial continuous generalised CDSN peeling skin syndrome peeling skin syndrome 1 PSS1 generalised peeling skin syndrome type B peeling skin syndrome type B generalized peeling skin syndrome type B generalised deciduous skin type B MONDO:0024548 Orphanet:263553 Any peeling skin syndrome in which the cause of the disease is a mutation in the CDSN gene. UMLS:C5679693 PSS OMIM:270300 PSS type B