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Disease Ontology Browser
peeling skin syndrome 6 (DOID:0070525)
Alliance: disease page
Synonyms: peeling skin syndrome type A; PSS6
Alt IDs: OMIM:618084
Definition: A peeling skin syndrome that has_material_basis_in homozygous mutation in the FLG2 gene on chromosome 1q21.3.

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)
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Send questions and comments to User Support. 		last database update
11/05/2024
MGI 6.24 		The Jackson Laboratory