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Summary Literature (0)
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 Disease Ontology (on Monarch Initiative):
MONDO:0002921 - longitudinal fissure


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

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