Any congenital muscular dystrophy in which the cause of the disease is a variation in the POMGNT2 gene.
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Ullrich congenital muscular dystrophy
MONDO:0000355
Bethlem myopathy
MONDO:0008029
arthrogryposis due to muscular dystrophy
MONDO:0009679
congenital muscular dystrophy-infantile cataract-hypogonadism syndrome
MONDO:0009680
muscular dystrophy, congenital, with rapid progression
MONDO:0009682
congenital myasthenic syndrome 10
MONDO:0009690