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

• GARD:12863
• MESH:C536316
• OMIM:609796
• ORDO:263534
• SNOMEDCT_US_2023_03_01:709416009
• UMLS_CUI:C1853354

Ontology

Human Disease   ( DOID:0070521 )