| Dataset | DISEASES Curated Gene-Disease Assocation Evidence Scores |
| Category | disease or phenotype associations |
| Type | disease |
| Description | A congenital structural myopathy characterized by generally non-progressive muscle weakness of varying severity; certain muscle fibers show the presence of rod-like structures called nemaline bodies. (Human Disease Ontology, DOID_3191) |
| Similar Terms | |
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8 genes involed in the disease nemaline myopathy from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
