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Echinobase
Summary Literature (0)
DOID:3191 - nemaline myopathy

Disease Ontology Definition: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.

Synonyms: Nemaline body disease, nemaline rod myopathy, rod myopathy,

Echinobase Genes :



Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): congenital structural myopathy (is_a)