Any congenital muscular dystrophy in which the cause of the disease is a variation in the POMGNT2 gene. The disease is Monarch Disease Ontology entry MONDO_0700075 (congenital muscular dystrophy caused by variation in POMGNT2). Also known as: congenital muscular dystrophy caused by mutation in POMGNT2, congenital muscular dystrophy-POMGNT2 related.