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Disease Ontology Browser
peeling skin syndrome (DOID:0060283)
Alliance: disease page
Alt IDs: OMIM:270300, OMIM:613088, ICD10CM:Q80.8, MESH:C564818, ORDO:263543
Definition: A skin disease that is characterized by the painless peeling of the top layer of skin predominately on the hands and feet, has_material_basis_in autosomal recessive inheritance of mutation in the TGM5 gene and/pr CSTA gene.

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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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last database update
MGI 6.22
The Jackson Laboratory