|
DOID:699 - mitochondrial myopathy
Disease Ontology Definition:A myopathy that is characterized by mitochondrial dysfunction.
Synonyms: mitochondrial cytopathy, mitochondrial cytopathy (disorder)
Xenbase Genes
:
polg,
yars2,
pus1,
rrm2b,
twnk,
slc25a4,
top3a,
dguok,
polg2,
rnaseh1,
dna2,
mt-co1,
chchd10,
mt-cyb,
mt-nd1,
| MONDO:0009637 - inborn mitochondrial myopathy |
| MIM:251900 - MITOCHONDRIAL MYOPATHY, EPISODIC, WITH OR WITHOUT OPTIC ATROPHY AND REVERSIBLE LEUKOENCEPHALOPATHY; MEOAL |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
myopathy (is_a)