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16q24.3 microdeletion syndrome

Disease Summary
Associated Targets (6)
Tbio

5

Tchem

1


GARD Rare
Mondo Description 16q24.3 microdeletion syndrome is a recently described syndrome associated with variable developmental delay, facial dysmorphism, seizures and autistic spectrum disorder.
Mondo Term and Equivalent IDs
MONDO:0016838:  16q24.3 microdeletion syndrome
GARD:0010935: 
Orphanet:261250: 
SCTID:719580004: 
UMLS:C4304594: 
UMLS:CN202174: