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DO Term : Cowden syndrome 4 [DOID:0081000] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A Cowden syndrome that has_material_basis_in heterozygous germline hypermethylation of the KLLN gene on chromosome 10q23.

synonyms:
OMIM:615107,
615107

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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