Term Name:	peeling skin syndrome 2
Synonyms:	acral peeling skin syndrome, APSS, localized peeling skin syndrome, PSS2
Definition:	A peeling skin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the TGM5 gene on chromosome 15q15.2.
Ontology:	Human Disease [DOID:0070521]   ( DOID:0070521 )