Human genes for nemaline myopathy 10
Nemaline myopathy 10 [DOID:0110931]
A nemaline myopathy characterized by early-onset generalized muscle weakness and hypotonia with respiratory insufficiency and feeding difficulties that has_material_basis_in homozygous or compound heterozygous mutation in the LMOD3 gene on chromosome 3p14.
Synonyms: nemaline myopathy 10, DOID:0110931, NEM10