disease arises from structure disease arises from alteration in structure predisposes towards 16p11.2 (Human) autism proximal 16p11.2 microdeletion syndrome https://github.com/monarch-initiative/mondo/issues/3664 https://github.com/monarch-initiative/mondo/issues/4521 https://rarediseases.info.nih.gov/diseases/10740/16p112-deletion-syndrome https://www.malacards.org/card/chromosome_16p112_deletion_syndrome_593_kb DOID:0070515 chromosome 16p11.2 deletion syndrome, 593kb autism susceptibility 14A Orphanet:261197 SCTID:699307007 ICD9:758.39 SCTID:718227006 microdeletion 16p11.2 proximal del(16)(p11.2) 16p11.2 deletion syndrome NCIT:C120408 GARD:0010740 UMLS:C3150154 MONDO:0012756 chromosome 16p11.2 deletion syndrome monosomy 16p11.2 A chromosomal anomaly characterized by developmental and language delays, mild intellectual disability, social impairments (autism spectrum disorders), mild variable dysmorphism and predisposition to obesity. MEDGEN:461504 MESH:C579850 proximal monosomy 16p11.2 OMIM:611913 Del(16)(p11.2) partial deletion of the short arm of chromosome 16