disease arises from structure disease arises from alteration in structure predisposes towards 15q11-q13 (Human) syndrome caused by partial chromosomal duplication syndromic disease epilepsy autism 15q11q13 microduplication syndrome https://github.com/monarch-initiative/mondo/issues/3492 https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/8993 https://www.malacards.org/card/15q11q13_microduplication_syndrome https://www.malacards.org/card/chromosome_15q11_q13_duplication_syndrome NCIT:C126692 chromosome 15q11-q13 DUPLICATION syndrome 15q11-q13 duplication syndrome SCTID:719427001 chromosome 15Q11.2 Duplication syndrome 15q11-q13 microduplication syndrome MONDO:0012081 Dup15q MEDGEN:390767 OMIM:608636 15q11q13 duplication syndrome trisomy 15q11-q13 The 15q11-q13 microduplication (dup15q11-q13) syndrome is characterized by neurobehavioral disorders, hypotonia, cognitive deficit, language delay and seizures. Prevalence is unknown. dup(15)(q11q13) UMLS:C2675336 GARD:0017172 autism, susceptibility to, 4 Orphanet:238446 Duplication 15Q11-q13 syndrome trisomy 15q11q13 autism susceptibility 4 partial duplication of the long arm of chromosome 15