inherited ichthyosis peeling skin syndrome https://github.com/monarch-initiative/mondo/issues/6749 https://github.com/monarch-initiative/mondo/issues/6877 https://www.malacards.org/card/peeling_skin_syndrome SCTID:239065004 MONDO:0019347 peeling skin disease UMLS:C1849193 OMIMPS:270300 familial continuous skin peeling syndrome GARD:0007347 keratosis exfoliativa congenita icd11.foundation:523640904 deciduous skin Orphanet:817 Peeling skin syndrome (PSS) refers to a group of rare autosomal recessive forms of ichthyosis that is characterized clinically by superficial, asymptomatic, spontaneous peeling of the skin and histologically by a shedding of the outer layers of the epidermis. PSS presents with either an acral (acral PSS) or a generalized distribution (generalized PSS type A (non inflammatory) or B (inflammatory)). Some cases remain difficult to classify, suggesting that there could be additional subtypes of PSS. familial continuous skin peeling MEDGEN:336530 DOID:0060283 PSS skin peeling syndrome NORD:1562 ICD9:757.39 idiopathic deciduous skin