OBO ID: DOID:0111269 |
Term Name: | autosomal dominant hyaline body myopathy | Search Ontology: | |
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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 | ||
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Ontology: | Human Disease ( DOID:0111269 ) |
OTHER autosomal dominant hyaline body myopathy PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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