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

Simpson-Golabi-Behmel syndrome

Disease Summary
Associated Targets (5)
Tbio

4

Tdark

1


Explore Associated Targets
Mondo Description Simpson-Golabi-Behmel syndrome is a rare X-linked multiple congenital anomalies syndrome, characterized by pre- and postnatal overgrowth, distinctive craniofacial features, variable congenital malformations, organomegaly and an increased tumor risk.
Mondo Term and Equivalent IDs
MONDO:0010731:  Simpson-Golabi-Behmel syndrome
GARD:0007649: 
MESH:C537340: 
NCIT:C131002: 
Orphanet:373: 
SCTID:439143004: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)
No novelty measurements found