|
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 - longitudinal fissure |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee