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DOID:422 - congenital structural myopathy
Disease Ontology Definition:A myopathy that is characterized by hypotonia, muscle weakness, and delayed development of motor skills.
Synonyms:
Xenbase Genes : tnnt1, acta1, neb, dnm2, klhl40, bin1, map3k20, mypn, kbtbd13, myf6, mtm1, cfl2, ryr1, lmod3, mtmr14,
MONDO:0002921 - congenital structural myopathy |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee