nemaline myopathy 10 (DOID:0110931)
Alliance: disease page
Synonyms: congenital myopathy 10; NEM10
Alt IDs: OMIM:616165
Definition: 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.