|Dataset||GAD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
3 genes associated with the disease nemaline myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.