disease arises from structure disease arises from alteration in structure 17q11.2 (Human) syndromic intellectual disability syndrome caused by partial chromosomal duplication hereditary disease 17q11.2 microduplication syndrome https://github.com/monarch-initiative/mondo/issues/3492 https://github.com/monarch-initiative/mondo/issues/4337 https://www.malacards.org/card/chromosome_17q112_duplication_syndrome_14_mb GARD:0016952 17q11.2 microduplication syndrome is characterized by dysmorphic features and intellectual deficit. Grisart-Destrée syndrome chromosome 17q11.2 duplication syndrome, 1.4-mb dup(17)(q11.2) trisomy 17q11.2 MEDGEN:501218 OMIM:618874 SCTID:719583002 MONDO:0015350 Nf1 Microduplication Syndrome Grisart-Destree syndrome UMLS:C3495679 Orphanet:139474 partial duplication of the long arm of chromosome 17