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Mitochondrial complex III deficiency
MONDO:0015448A rare, genetic, mitochondrial oxidative phosphorylation disorder characterized by a wide spectrum of clinical manifestations ranging from isolated myopathy or transient hepatopathy to severe multisystem disorder (that may include hypotonia, failure to thrive, psychomotor delay, cardiomyopathy, encephalopathy, renal tubulopathy, hearing impairment, lactic acidosis, hypoglycemia and other signs and symptoms).
Also known as: isolated CoQ-cytochrome C reductase deficiency, isolated coenzyme Q-cytochrome C reductase deficiency, isolated mitochondrial respiratory chain complex III deficiency, isolated ubiquinone-cytochrome C reductase deficiency, mitochondrial respiratory chain complex III deficiency, isolated complex III deficiency
13 clinical trials for this condition and its sub-types, 0 tagged with Mitochondrial complex III deficiency itself.
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Browse by category →Sub-types of Mitochondrial complex III deficiency
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11 sub-types
- Mitochondrial complex III deficiency nuclear type 1 0 trials Sub-types →
- Mitochondrial complex III deficiency nuclear type 2 0 trials
- Mitochondrial complex III deficiency nuclear type 3 0 trials
- Mitochondrial complex III deficiency nuclear type 4 0 trials
- Mitochondrial complex III deficiency nuclear type 5 0 trials
- Mitochondrial complex III deficiency nuclear type 6 0 trials
- Mitochondrial complex III deficiency nuclear type 7 0 trials
- Mitochondrial complex III deficiency nuclear type 8 0 trials
- Mitochondrial complex III deficiency nuclear type 9 0 trials
- Mitochondrial complex III deficiency, nuclear type 10 0 trials
- Mitochondrial complex III deficiency, nuclear type 11 0 trials
Most studied deeper sub-types
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