Search Ontology:
Human Disease

peeling skin syndrome 1

Term ID
DOID:0070520
Synonyms
  • generalized inflammatory peeling skin syndrome
  • inflammatory peeling skin syndrome
  • peeling skin syndrome type B
  • PSS1
Definition
A peeling skin syndrome that has_material_basis_in homozygous mutation in the CDSN gene on chromosome 6p21.33. (2)
References
  • MIM:270300
  • ORDO:263553
  • UMLS_CUI:C5679693
  • UMLS_CUI:C5768235
Ontology
Human Disease   ( DOID:0070520 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models