nemaline myopathy 11 (DOID:0110933)
Alliance: disease page
Synonyms: NEM11; nemaline myopathy 11, autosomal recessive
Alt IDs: OMIM:617336
Definition: A nemaline myopathy characterized by onset of slowly progressive muscle weakness in the first decade of life that has_material_basis_in homozygous or compound heterozygous mutation in the MYPN gene on chromosome 10q21.