syndromic intellectual disability multiple congenital anomalies/dysmorphic syndrome-intellectual disability multiple congenital anomalies due to 14q32.2 maternally expressed gene defect https://github.com/monarch-initiative/mondo/issues/4069 https://github.com/monarch-initiative/mondo/issues/5588 https://github.com/monarch-initiative/mondo/issues/6125 https://github.com/monarch-initiative/mondo/issues/6127 DOID:0111712 GARD:0017219 MCA due to 14q32.2 maternally expressed gene defect UMLS:C5779872 Orphanet:254519 A rare genetic disease characterized by polyhydramnios (mostly due to placentomegaly), fetal macrosomia, abdominal wall defects, skeletal abnormalities (including bell-shaped thorax, coat-hanger appearance of the ribs and decreased mid to wide thorax diameter ratio in infancy), feeding difficulties and impaired swallowing, dysmorphic features (hairy forehead, full cheeks, protruding philtrum, micrognathia), developmental delay and intellectual disability. Additional features may include kyphoskoliosis, joint contractures, diastasis recti, muscular hypotonia. There is increased risk of hepatoblastoma. MONDO:0016779 MEDGEN:1830421 Kagami-Ogata syndrome multiple congenital anomalies due to 14q32.2 imprinting defect