disease arises from structure disease arises from alteration in structure 2p13.2 (Human) syndromic intellectual disability syndrome caused by partial chromosomal deletion multiple congenital anomalies/dysmorphic syndrome-intellectual disability partial deletion of the short arm of chromosome 2 2p13.2 microdeletion syndrome https://github.com/monarch-initiative/mondo/issues/3664 https://www.malacards.org/card/2p132_microdeletion_syndrome Del(2)(p13.2) 2p13.2 microdeletion syndrome is a rare partial autosomal monosomy characterized by global development delay, intellectual disability, behavioral abnormalities (hyperactivity, attention deficit and autistic behaviors), brachycephaly and variable facial dysmorphism. Other associated features may include vertebral fusions, mild contractures of knees and elbows, and feeding difficulties during infancy. MONDO:0018207 MEDGEN:1662313 Orphanet:363680 GARD:0021557 UMLS:C4749460