Human genes for nemaline myopathy 11
Nemaline myopathy 11 [DOID:0110933]
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.
Synonyms: nemaline myopathy 11, DOID:0110933, NEM11, nemaline myopathy 11, autosomal recessive, autosomal recessive nemaline myopathy 11 ...