FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term peeling skin syndrome 2 ID (Ontology) DOID:0070521 (Human Disease)
Definition A peeling skin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the TGM5 gene on chromosome 15q15.2.
Also Known As "PSS2"
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 Genes
 peeling skin syndrome 2       1
 for disease ribbon | peeling skin syndrome 2       1
 model of | peeling skin syndrome 2       1
Spanning Tree (Parents/Children)
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autosomal recessive disease__
skin disease_________________|
                             peeling skin syndrome
                              |__peeling skin syndrome 2  1 rec.
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Is a peeling skin syndrome
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Synonyms
  • "acral peeling skin syndrome" BROAD
    "APSS" BROAD OMO:0003012
    "localized peeling skin syndrome" BROAD
    "PSS2" EXACT OMO:0003012
Secondary IDs
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GARD:12863
MESH:C536316
MIM:609796
ORDO:263534
SNOMEDCT_US_2023_03_01:709416009
UMLS_CUI:C1853354