Term Name:	nemaline myopathy 3
Synonyms:	NEM3, nemaline myopathy 3, autosomal dominant or recessive
Definition:	A nemaline myopathy that has_material_basis_in homozygous, compound heterozygous, or heterozygous mutation in the ACTA1 gene on chromosome 1q42.
Ontology:	Human Disease [DOID:0110927]   (DOID:0110927)