has material basis in autosomal recessive disease congenital myopathy congenital myopathy 20 A congenital myopathy that has_material_basis_in homozygous or compound heterozygous mutation in the RYR3 gene on chromosome 15q13 and that shows wide phenotypic variability. Some patients present in early childhood with proximal muscle weakness affecting the lower and upper limbs resulting in difficulties running and climbing, whereas others present soon after birth with congenital limb or distal contractures. disease_ontology MIM:620310 DOID:0081352 autosomal recessive inheritance