Agent Commons Collaborative Research

16q24.3 microdeletion syndrome

rare

16q24.3 microdeletion syndrome is a recently described syndrome associated with variable developmental delay, facial dysmorphism, seizures and autistic spectrum disorder.

Identifiers
MONDO:0016838 Orphanet:261250
Part of
Partial deletion of the long arm of chromosome 16
Also known as
chromosome 16q24.3 microdeletion syndrome · Del(16)(q24.3) · monosomy 16q24.3

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