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

20p12.3 microdeletion syndrome

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description 20p12.3 microdeletion syndrome is a recently described syndrome characterized by Wolff-Parkinson-White syndrome, variable developmental delay and facial dysmorphism.
Mondo Term and Equivalent IDs
MONDO:0016841:  20p12.3 microdeletion syndrome
GARD:0012492: 
Orphanet:261295: 
SCTID:719650004: 
UMLS:C4304539: 
UMLS:CN202180: