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DO Term : peeling skin syndrome 3 [DOID:0070522] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A peeling skin syndrome that has_material_basis_in autosomal recessive inheritance of variation in the chromosome region 19q13.

synonyms:
OMIM:616265,
peeling skin syndrome type A,
PSS3,
616265

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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