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Disease Ontology Browser
peeling skin syndrome 3 (DOID:0070522)
Alliance: disease page
Synonyms: peeling skin syndrome type A; PSS3
Alt IDs: OMIM:616265
Definition: A peeling skin syndrome that has_material_basis_in autosomal recessive inheritance of variation in the chromosome region 19q13.

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
11/19/2024
MGI 6.24 		The Jackson Laboratory