OBO ID: DOID:0080097 |
Term Name: | myofibrillar myopathy 6 | Search Ontology: | |
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Definition: | A myofibrillar myopathy that has_material_basis_in heterozygous mutation in the BAG3 gene on chromosome 10q26. https://www.omim.org/entry/612954 | ||
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Ontology: | Human Disease ( DOID:0080097 ) |
OTHER myofibrillar myopathy 6 PAGES
ZEBRAFISH MODELS
PHENOTYPE
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CITATIONS (2)
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