FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term autosomal recessive hyaline body myopathy ID (Ontology) DOID:0111268 (Human Disease)
Definition A hyaline body myopathy that has_material_basis_in compound heterozygous or homozygous mutation in MYH7 on 14q11.2.
Also Known As "autosomal recessive myosin storage congenital myopathy 7B" ; "congenital myopathy 7B" ; "MSMB" (for all, see Synonyms field below)
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
    Results list data from multiple species. Click on a button above and use the 'Filter by species' options on the resulting HitList to retrieve species-specific data.
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
 Full annotation statements 
Relevant FlyBase reports
 Genes
 autosomal recessive hyaline body myopathy       1
 for disease ribbon | autosomal recessive hyaline body myopathy       1
 model of | autosomal recessive hyaline body myopathy       1
Spanning Tree (Parents/Children)
Only view relationship: 
autosomal genetic disease
 |__autosomal recessive disease__
congenital myopathy              |
 |__hyaline body myopathy________|
                                 autosomal recessive hyaline body myopathy  1 rec.
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal recessive disease
hyaline body myopathy
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "autosomal recessive myosin storage congenital myopathy 7B" EXACT
    "congenital myopathy 7B" EXACT
    "MSMB" EXACT OMO:0003012
    "Myopathy, myosin storage, autosomal recessive" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
MIM:255160