Search Ontology:
Human Disease

peeling skin syndrome 2

Term ID
DOID:0070521
Synonyms
  • acral peeling skin syndrome
  • APSS
  • localized peeling skin syndrome
  • PSS2
Definition
A peeling skin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the TGM5 gene on chromosome 15q15.2. (3)
References
Ontology
Human Disease   ( DOID:0070521 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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