Cowden syndrome 4 Disease Ontology Browser

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Disease Ontology Browser

Cowden syndrome 4 (DOID:0081000)
Alliance: disease page
Alt IDs: OMIM:615107
Definition: A Cowden syndrome that has_material_basis_in heterozygous germline hypermethylation of the KLLN gene on chromosome 10q23.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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