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DO Term : peeling skin syndrome 5 [DOID:0070524] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A peeling skin syndrome that has_material_basis_in homozygous mutation in the SERPINB8 gene on chromosome 18q22.1.

synonyms:
exfoliative ichthyosis,
617115,
PSS5,
autosomal recessive exfoliative ichthyosis,
OMIM:617115,
ichthyosis exfoliativa

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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