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Cowden disease

Disease Summary
Associated Targets (12)
Tbio

5

Tchem

4

Tclin

3


GARD Rare
Disease Ontology Description 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.
Mondo Term and Equivalent IDs
MONDO:0016063:  Cowden disease
GARD:0006202: 
MESH:D006223: 
NCIT:C3076: 
OMIMPS:158350: 
Orphanet:201: 
SCTID:58037000: 
UMLS:C0018553: