Search Ontology:
Human Disease

myofibrillar myopathy 5

Term ID
DOID:0080096
Synonyms
  • filaminopathy
Definition
A myofibrillar myopathy that has_material_basis_in heterozygous mutation in the FLNC gene on chromosome 7q32. https://www.omim.org/entry/609524
References
Ontology
Human Disease   ( DOID:0080096 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models
Citations