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Summary Literature (0)
DOID:0081337 - congenital myopathy

Disease Ontology Definition:A myopathy that is characterized by hypotonia and weakness, usually present from birth.

Synonyms:

Xenbase Genes : tnnt1, cntn1, acta1, megf10, neb, dnm2, klhl40, bin1, map3k20, mypn, kbtbd13, myh7l, myf6, mtm1, cfl2, [+]



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

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