Search Ontology:
Human Disease

myofibrillar myopathy 6

Term ID
DOID:0080097
Synonyms
  • BAG3-related myofibrillar myopathy
Definition
A myofibrillar myopathy that has_material_basis_in heterozygous mutation in the BAG3 gene on chromosome 10q26. https://pubmed.ncbi.nlm.nih.gov/22734908/
References
Ontology
Human Disease   ( DOID:0080097 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models