Term Name:	nemaline myopathy 11
Synonyms:	NEM11, nemaline myopathy 11, autosomal recessive
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.
Ontology:	Human Disease [DOID:0110933]   ( DOID:0110933 )