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DO Term : peeling skin syndrome 6 [DOID:0070525] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A peeling skin syndrome that has_material_basis_in homozygous mutation in the FLG2 gene on chromosome 1q21.3.

synonyms:
618084,
peeling skin syndrome type A,
OMIM:618084,
PSS6

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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