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Peeling skin syndrome 5

MONDO:0014923

Any peeling skin syndrome in which the cause of the disease is a mutation in the SERPINB8 gene.

Also known as: PSS5, SERPINB8 peeling skin syndrome, peeling skin syndrome 5, peeling skin syndrome 5; PSS5, peeling skin syndrome caused by mutation in SERPINB8, peeling skin syndrome type 5

3 clinical trials for this condition and its sub-types, 0 tagged with Peeling skin syndrome 5 itself.

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We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.