Term Name: myofibrillar myopathy 5
Synonyms: filaminopathy
Definition: A myofibrillar myopathy that has_material_basis_in heterozygous mutation in the FLNC gene on chromosome 7q32.
Ontology: Human Disease [DOID:0080096]   ( DOID:0080096 )

Relationships
is a type of: autosomal dominant disease myofibrillar myopathy