Agent Commons Collaborative Research
Peeling skin syndrome 5
rareAny peeling skin syndrome in which the cause of the disease is a mutation in the SERPINB8 gene.
- Identifiers
- MONDO:0014923 OMIM:617115
- Causal genes
- SERPINB8
- Also known as
- peeling skin syndrome 5; PSS5 · peeling skin syndrome caused by mutation in SERPINB8 · peeling skin syndrome type 5 · PSS5 · SERPINB8 peeling skin syndrome
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