Search Ontology:
Human Disease

autosomal recessive hyaline body myopathy

Term ID
DOID:0111268
Synonyms
  • congenital myopathy 7B
  • MSMB
  • Myopathy, myosin storage, autosomal recessive
Definition
A hyaline body myopathy that has_material_basis_in compound heterozygous or homozygous mutation in MYH7 on 14q11.2. https://www.ncbi.nlm.nih.gov/pubmed/17372140
References
Ontology
Human Disease   ( DOID:0111268 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models