Category:Mitochondrial diseases
From WikiMD's Wellness Encyclopedia
Pages in category "Mitochondrial diseases"
The following 155 pages are in this category, out of 155 total.
B
C
- Cerebellar ataxia infantile with progressive external ophthalmoplegia
- CHCHD10
- CHCHD2
- Chronic progressive external ophthalmoplegia
- COA3
- COA5
- COA6
- Coenzyme Q cytochrome c reductase deficiency of
- Coenzyme Q10 deficiency
- Complex 1 mitochondrial respiratory chain deficiency
- Complex 2 mitochondrial respiratory chain deficiency
- Complex 3 mitochondrial respiratory chain deficiency
- Complex 4 mitochondrial respiratory chain deficiency
- Complex 5 mitochondrial respiratory chain deficiency
- COQ9
- COX20
- COX4I2
- COX6A2
- COX6B1
- COX6B2
- COX8A
- Cytochrome C oxidase deficiency
- Cytochrome-c oxidase deficiency
L
M
- MELAS syndrome
- Merrf syndrome
- MERRF syndrome
- MERTK
- MILS syndrome
- Mitochondrial complex II deficiency
- Mitochondrial cytopathy (generic term)
- Mitochondrial diseases of nuclear origin
- Mitochondrial diseases, clinically undefinite
- Mitochondrial DNA depletion syndrome
- Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria
- Mitochondrial DNA-associated Leigh syndrome
- Mitochondrial encephalomyopathy
- Mitochondrial encephalomyopathy aminoacidopathy
- Mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes
- Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes
- Mitochondrial genetic disorders
- Mitochondrial myopathy
- Mitochondrial myopathy lactic acidosis
- Mitochondrial myopathy-encephalopathy-lactic acidosis
- Mitochondrial neurogastrointestinal encephalopathy syndrome
- Mitochondrial replacement therapy
- MNGIE syndrome
- MPV17-related hepatocerebral mitochondrial DNA depletion syndrome
- MT-ATP6
- MT-RNR1
- MT-TD
- MT-TH
- MT-TL1
- MT-TP
- MT-TR
- MT-TS1
- MT-TS2
- MT-TV (mitochondrial)
- Myoclonic epilepsy with ragged red fibers
- Myoclonic epilepsy with ragged red fibres
- Myopathy ophthalmoplegia hypoacousia areflexia
N
- NADH CoQ reductase, deficiency of
- NADH dehydrogenase (ubiquinone), alpha 1
- NDUFA11
- NDUFA13
- NDUFA3
- NDUFA4
- NDUFA4L2
- NDUFA6
- NDUFA7
- NDUFA8
- NDUFA9
- NDUFAF1
- NDUFAF2
- NDUFAF3
- NDUFAF4
- NDUFAF5
- NDUFAF7
- NDUFAF8
- NDUFB1
- NDUFB10
- NDUFB6
- NDUFB7
- NDUFS1
- NDUFS2
- NDUFS4
- NDUFS8
- NDUFV1
- NDUFV2
- Necrotizing encephalopathy, infantile subacute
- Neuropathy ataxia retinitis pigmentosa syndrome
- Neuropathy, ataxia, and retinitis pigmentosa
