You are using an outdated browser. Please upgrade your browser to improve your experience.

PTEN hamartoma tumor syndrome

Disease Summary
Associated Targets (12)
Tbio

5

Tchem

4

Tclin

3


Explore Associated Targets
Mondo Description A group of clinically heterogeneous disorders united by a germline PTEN mutation and the involvement of derivatives of all 3 germ cell layers, manifesting with hamartomas, overgrowth and neoplasia. Currently, subsets carrying clinical diagnoses of Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome, Proteus and Proteus-like syndromes and SOLAMEN syndrome belong to PHTS.
Mondo Term and Equivalent IDs
MONDO:0017623:  PTEN hamartoma tumor syndrome
GARD:0012800: 
Orphanet:306498: 
SCTID:722859001: 
UMLS:C1959582: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found