Human genes for nemaline myopathy 2
Nemaline myopathy 2 [DOID:0110928]
A nemaline myopathy that has_material_basis_in homozygous or compound heterozygous mutation in the NEB gene on chromosome 2q23.
Synonyms: nemaline myopathy 2, DOID:0110928, NEM2, nemaline myopathy 2, autosomal recessive, autosomal recessive nemaline myopathy 2 ...