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Disease Ontology Browser
peeling skin syndrome 2 (DOID:0070521)
Alliance: disease page
Synonyms: acral peeling skin syndrome; APSS; localized peeling skin syndrome; PSS2
Alt IDs: OMIM:609796, MESH:C536316, ORDO:263534, UMLS_CUI:C1853354
Definition: A peeling skin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the TGM5 gene on chromosome 15q15.2.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory