Term Name:	nemaline myopathy 10
Synonyms:	congenital myopathy 10, NEM10
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.
Ontology:	Human Disease [DOID:0110931]   ( DOID:0110931 )