Search Ontology:
Human Disease

autosomal dominant hyaline body myopathy

Term ID
DOID:0111269
Synonyms
  • congenital myopathy 7A
  • MSMA
  • myopathy with lysis of type I myofibrils
  • Myopathy, myosin storage, autosomal dominant
Definition
A hyaline body myopathy that has_material_basis_in heterozygous mutation in MYH7 on 14q11.2. https://www.ncbi.nlm.nih.gov/pubmed/16684601
References
Ontology
Human Disease   ( DOID:0111269 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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