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

Disease Ontology Definition:A congenital myopathy characterized by generally non-progressive muscle weakness of varying severity and problems with the tone and contraction of skeletal muscles. The muscle cells contain abnormal clumps of threadlike material called nemaline bodies.

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

Echinobase Genes :



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

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