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DO Term : peeling skin syndrome 2 [DOID:0070521] Disease Ontology
Namespace  disease_ontology Obsolete  false
description  A peeling skin syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the TGM5 gene on chromosome 15q15.2.
  • synonyms:
  • 609796,
  • UMLS_CUI:C1853354,
  • APSS,
  • acral peeling skin syndrome,
  • SNOMEDCT_US_2023_03_01:709416009,
  • PSS2,
  • MESH:C536316,
  • ORDO:263534,
  • OMIM:609796,
  • GARD:12863,
  • localized peeling skin syndrome
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents





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