Proximal 16p11.2 microdeletion syndrome

A chromosomal anomaly characterized by developmental and language delays, mild intellectual disability, social impairments (autism spectrum disorders), mild variable dysmorphism and predisposition to obesity.

Also known as: autism susceptibility 14A, chromosome 16p11.2 deletion syndrome, 593kb, proximal del(16)(p11.2), proximal monosomy 16p11.2, 16p11.2 deletion syndrome, Del(16)(p11.2), autism, susceptibility to, 14A, chromosome 16p11.2 deletion syndrome

1 clinical trial for this condition and its sub-types, 1 tagged with Proximal 16p11.2 microdeletion syndrome itself.