nemaline myopathy Gene Set

Dataset GAD Gene-Disease Associations
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
Downloads & Tools


3 genes associated with the disease nemaline myopathy in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
TPM1 tropomyosin 1 (alpha)
TPM3 tropomyosin 3
TPMT thiopurine S-methyltransferase