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Summary Literature (0)
DOID:0070521 - peeling skin syndrome 2

Disease Ontology Definition:A peeling skin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the TGM5 gene on chromosome 15q15.2.

Synonyms: acral peeling skin syndrome, APSS, localized peeling skin syndrome, PSS2

Xenbase Genes : tgm5


MIM:
MIM:609796 - PEELING SKIN SYNDROME 2; PSS2

Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): peeling skin syndrome (is_a)