OBO ID: DOID:0111268
Term Name: autosomal recessive hyaline body myopathy Search Ontology:
Synonyms:
  • 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)
OTHER autosomal recessive hyaline body myopathy PAGES
GENES INVOLVED
Human Gene Zebrafish Ortholog OMIM Term OMIM Phenotype ID
MYH7 Myopathy, myosin storage, autosomal recessive 255160
ZEBRAFISH MODELS No data available
PHENOTYPE No data available

CITATIONS: None