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Metadata
ID	DOID:0080096
Name	myofibrillar myopathy 5
Definition	A myofibrillar myopathy that has_material_basis_in heterozygous mutation in the FLNC gene on chromosome 7q32. https://pubmed.ncbi.nlm.nih.gov/15929027/
Xrefs	MIM:609524
Synonyms	filaminopathy [EXACT]
Parent Relationships	is_a myofibrillar myopathy is_a autosomal dominant disease
Subclass Logical Relationships	has material basis in some autosomal dominant inheritance