Catalog

16p11.2 deletion

No MMS code

Link to WHO Definition

16p11.2 deletion – http://id.who.int/icd/entity/1398449020

The proximal 16p11.2 microdeletion syndrome is a chromosomal anomaly characterised by developmental and language delays, mild intellectual disability, social impairments (autism spectrum disorders), mild variable dysmorphism and predisposition to obesity.