Disease Index
9,486 diseasesmitochondrial DNA depletion syndrome
human disease
ICD: G71.3
mitochondrial DNA depletion syndrome 1
Human disease
MeSH: C536350
mitochondrial DNA depletion syndrome 11
Human disease
mitochondrial DNA depletion syndrome 12b
human disease
mitochondrial DNA depletion syndrome 13
Human disease
mitochondrial DNA depletion syndrome 2
Human disease
MeSH: C563698
mitochondrial DNA depletion syndrome 3
Human disease
MeSH: C580039
mitochondrial DNA depletion syndrome 4b
Human disease
mitochondrial DNA depletion syndrome 5
Human disease
MeSH: C567624
mitochondrial DNA depletion syndrome 6
Human disease
MeSH: C538344
mitochondrial DNA depletion syndrome 8a
Human disease
MeSH: C536350
mitochondrial DNA depletion syndrome 9
Human disease
MeSH: C580473
mitochondrial DNA depletion syndrome, encephalomyopathic form
human disease
mitochondrial DNA depletion syndrome, hepatocerebral form
human disease
MeSH: C580039
mitochondrial DNA depletion syndrome, hepatocerebrorenal form
human disease
mitochondrial DNA maintenance syndrome
acquired metabolic disease that is has its basis in the disruption of mitochondrial genome maintenance
mitochondrial membrane transport disorder
human disease
mitochondrial myopathy
myopathy characterized by mitochondrial dysfunction
ICD: G71.3MeSH: D017240
mitochondrial myopathy with reversible cytochrome c oxidase deficiency
human disease
mitochondrial neurogastrointestinal encephalomyopathy
Mitochondrial NeuroGastroIntestinal Encephalomyopathy (MNGIE) syndrome is characterized by the association of gastrointestinal dysmotility, peripheral neuropathy, chronic progressive external ophthalmoplegia and leukoencephalopathy
MeSH: C537477
mitochondrial non-syndromic sensorineural deafness
human disease
mitochondrial non-syndromic sensorineural deafness with susceptibility to aminoglycoside exposure
human disease
MeSH: C564013
mitochondrial oxidative phosphorylation disorder
human disease
mitochondrial oxidative phosphorylation disorder due to a duplication of mitochondrial DNA
human disease
mitochondrial oxidative phosphorylation disorder due to a large-scale single deletion of mitochondrial DNA
human disease
mitochondrial oxidative phosphorylation disorder due to a point mutation of mitochondrial DNA
human disease
mitochondrial oxidative phosphorylation disorder due to mitochondrial DNA anomalies
human disease
mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies
mitochondrial oxidative phosphorylation disorder with no known mechanism
human disease
mitochondrial protein import disorder
human disease