About   Help   FAQ
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory