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Mitochondrial respiratory chain complex deficiency
MONDO:0000066A mitochondrial energy metabolism disorder where respiratory complex (I–V) is dysfunctional, typically due to mutations in genes encoding that specific complex’s proteins or assembly factors.
Also known as: isolated oxidative phosphorylation complex disorder, mitochondrial complex deficiency
16 clinical trials for this condition and its sub-types, 4 tagged with Mitochondrial respiratory chain complex deficiency itself.
Follow this condition to get notified about new trialsWhere it sits in the disease tree
Browse by category →Sub-types of Mitochondrial respiratory chain complex deficiency
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Mitochondrial complex I deficiency 2 trials
2 sub-types
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22 sub-types
- COX deficiency, benign infantile mitochondrial myopathy 0 trials
- Mitochondrial complex 4 deficiency, nuclear type 25 0 trials
- Mitochondrial complex IV deficiency, nuclear type 1 0 trials
- Mitochondrial complex IV deficiency, nuclear type 10 0 trials
- Mitochondrial complex IV deficiency, nuclear type 11 0 trials
- Mitochondrial complex IV deficiency, nuclear type 12 0 trials
- Mitochondrial complex IV deficiency, nuclear type 14 0 trials
- Mitochondrial complex IV deficiency, nuclear type 15 0 trials
- Mitochondrial complex IV deficiency, nuclear type 16 0 trials
- Mitochondrial complex IV deficiency, nuclear type 17 0 trials
- Mitochondrial complex IV deficiency, nuclear type 18 0 trials
- Mitochondrial complex IV deficiency, nuclear type 19 0 trials
- Mitochondrial complex IV deficiency, nuclear type 20 0 trials
- Mitochondrial complex IV deficiency, nuclear type 21 0 trials
- Mitochondrial complex IV deficiency, nuclear type 22 0 trials
- Mitochondrial complex IV deficiency, nuclear type 23 0 trials
- Mitochondrial complex IV deficiency, nuclear type 24 0 trials
- Mitochondrial complex IV deficiency, nuclear type 3 0 trials
- Mitochondrial complex IV deficiency, nuclear type 4 0 trials
- Mitochondrial complex IV deficiency, nuclear type 7 0 trials
- Mitochondrial complex IV deficiency, nuclear type 8 0 trials
- Pancreatic insufficiency-anemia-hyperostosis syndrome 0 trials
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SDHC-related Mitochondrial Disease 0 trials
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Mitochondrial complex III deficiency 0 trials
1 sub-type
Most studied deeper sub-types
Leber hereditary optic neuropathy, autosomal recessive
(0)
Leber-like hereditary optic neuropathy, autosomal recessive 1
(0)
Leber-like hereditary optic neuropathy, autosomal recessive 2
(0)
Mitochondrial complex I deficiency, mitochondrial type 1
(0)
Mitochondrial complex I deficiency, nuclear type 1
(0)
Mitochondrial complex I deficiency, nuclear type 10
(0)
Mitochondrial complex I deficiency, nuclear type 11
(0)
Mitochondrial complex I deficiency, nuclear type 12
(0)
Mitochondrial complex I deficiency, nuclear type 13
(0)
Mitochondrial complex I deficiency, nuclear type 14
(0)
Mitochondrial complex I deficiency, nuclear type 15
(0)
Mitochondrial complex I deficiency, nuclear type 16
(0)
Mitochondrial complex I deficiency, nuclear type 17
(0)
Mitochondrial complex I deficiency, nuclear type 18
(0)
Mitochondrial complex I deficiency, nuclear type 19
(0)
Mitochondrial complex I deficiency, nuclear type 2
(0)
Mitochondrial complex I deficiency, nuclear type 21
(0)
Mitochondrial complex I deficiency, nuclear type 22
(0)
Mitochondrial complex I deficiency, nuclear type 23
(0)
Mitochondrial complex I deficiency, nuclear type 24
(0)