syndromic intellectual disability multiple congenital anomalies/dysmorphic syndrome-intellectual disability 19p13.3 microduplication syndrome https://github.com/monarch-initiative/mondo/issues/3492 https://www.malacards.org/card/19p133_microduplication_syndrome GARD:0021875 MEDGEN:1807189 dup(19)(p13.13) MONDO:0018658 19p13.3 microduplication syndrome is a rare, genetic, syndromic intellectual disability characterized by intrauterine growth retardation, microcephaly, hypotonia, motor and neurodevelopmental delay, speech delay, intellectual disability, and mild dysmorphic features. UMLS:C5679996 Orphanet:447980 partial duplication of the short arm of chromosome 19