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Summary Literature (0)
DOID:0070522 - peeling skin syndrome 3

Disease Ontology Definition:A peeling skin syndrome that has_material_basis_in autosomal recessive inheritance of variation in the chromosome region 19q13.

Synonyms: peeling skin syndrome type A, PSS3

Xenbase Genes : chst8



Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): peeling skin syndrome (is_a)