Human genes for peeling skin syndrome
Peeling skin syndrome [DOID:0060283]
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.
Synonyms: peeling skin syndrome, DOID:0060283, peeling skin disease, peeling skin disorder, peeling skin syndromes