multiple congenital anomalies due to 14q32.2 paternally expressed gene defect
MONDO:0100507Mondo
Findings
No curated finding names multiple congenital anomalies due to 14q32.2 paternally expressed gene defect yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
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).
Definition from the Mondo Disease Ontology (MONDO:0100507), read 2026-09-29. CC BY 4.0.