Search Ontology:
Human Disease

peeling skin syndrome 5

Term ID
DOID:0070524
Synonyms
  • autosomal recessive exfoliative ichthyosis
  • exfoliative ichthyosis
  • ichthyosis exfoliativa
  • PSS5
Definition
A peeling skin syndrome that has_material_basis_in homozygous mutation in the SERPINB8 gene on chromosome 18q22.1. https://pubmed.ncbi.nlm.nih.gov/27476651/
References
Ontology
Human Disease   ( DOID:0070524 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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