myofibrillar myopathy 11 (DOID:0081338)
Alliance: disease page
Alt IDs: OMIM:619178
Definition: A myofibrillar myopathy that is characterized by onset of slowly progressive proximal muscle weakness in the first decade of life and that has_material_basis_in homozygous or compound heterozygous mutation in the UNC45B gene on chromosome 17q11.