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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, myh7, 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)