congenital muscular dystrophy Ullrich congenital muscular dystrophy A congenital muscular dystrophy that is characterized by muscle weakness and respiratory depression and has_material_basis_in mutation in the COL6A1, COL6A2 and COL6A3 that produce components of type VI collagen. GARD:4769 OMIM mapping confirmed by DO. [SN]. OMIM:254090 ULLRICH DISEASE Ullrich scleroatonic muscular dystrophy disease_ontology DOID:0050558 autosomal dominant disease autosomal recessive disease