disease arises from structure disease arises from alteration in structure 16p13.2 (Human) Hao-Fountain syndrome partial deletion of the short arm of chromosome 16 Hao-Fountain syndrome due to 16p13.2 microdeletion Del(16)(p13.2) chromosome 16P13.2 deletion syndrome MONDO:0100528 MEDGEN:1804697 GARD:0017920 chromosome 16p13.2 deletion syndrome A partial deletion of the short arm of chromosome 16 characterized by developmental delay, intellectual disability, speech delay, autism spectrum disorder, epilepsy, hypogonadism, and hypotonia. The behavioral profile includes impulsivity, compulsivity, stubbornness, manipulative behaviors, temper tantrums, and aggressive behaviors. Orphanet:500055 UMLS:C5680086 16p13.2 microdeletion syndrome monosomy 16p13.2