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Chromosome 16p12.2-p11.2 deletion syndrome

rare

16p11.2-p12.2 microdeletion syndrome is a recently described syndrome characterized by developmental delay and facial dysmorphism.

Identifiers
MONDO:0013320 OMIM:613604Orphanet:261211
Part of
Partial deletion of the short arm of chromosome 16
Also known as
16p11.2-p12.2 microdeletion syndrome · 16p11.2p12.2 microdeletion syndrome · chromosome 16p12.2-p11.2 deletion syndrome, isolated cases · Del(16)(p11.2p12.2) · monosomy 16p11.2-p12.2

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