multiple congenital anomalies due to 14q32.2 imprinting defect multiple congenital anomalies due to 14q32.2 paternally expressed gene defect https://github.com/monarch-initiative/mondo/issues/6129 GARD:0026256 Temple syndrome Temple syndrome is a less specific phenotype including intrauterine and postnatal growth restriction, hypotonia, feeding difficulties in infancy, truncal obesity, and small feet and hands. Temple syndrome is caused by defects or absence of paternally derived imprinting signals (including maternal UPD14). MONDO:0100507