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Disease Ontology Browser
Cowden disease (DOID:6457)
Alliance: disease page
Synonyms: dysplastic Gangliocytoma of Cerebellum; Lhermitte-Duclos disease (disorder); multiple hamartoma syndrome
Alt IDs: OMIM:158350, OMIM:612359, OMIM:615106, OMIM:615107, OMIM:615108, OMIM:615109, DOID:3471, MESH:D006223, NCI:C3076, NCI:C8419, ORDO:201, UMLS_CUI:C0018553, UMLS_CUI:C0391826
Definition: An autosomal dominant disease characterized by multiple noncancerous, tumor-like growths (hamartomas) and an increased risk of certain forms of cancer, especially breast, thyroid and endometrium. It is caused by mutations in the PTEN, SDHB, SDHD and KLLN genes.

Disease References using Mouse Models (11)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/28/2017
MGI 6.11
The Jackson Laboratory