Term Name:	myofibrillar myopathy 10
Synonyms:	MFM10
Definition:	A myofibrillar myopathy characterized by onset of muscle pain, cramping, and exercise fatigue in the first or second decades of life that has_material_basis_in homozygous or compound heterozygous mutation in the SVIL gene on chromosome 10p11.23.
Ontology:	Human Disease [DOID:0112108]   ( DOID:0112108 )