Coenzyme Q10 deficiency
Coenzyme Q10 deficiency |
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Ubiquinone |
Classification and external resources |
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OMIM |
607426 |
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Coenzyme Q10 deficiency is a deficiency of Coenzyme Q10.
It can be associated with COQ2, APTX, PDSS2, PDSS1, CABC1, and COQ9.[1]
Some forms may be more treatable than other mitochondrial diseases.[2]
References
Disorders of TCA and ETC |
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| Citric acid cycle | |
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| Electron transport chain | |
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| Description |
- Metabolism
- Enzymes and pathways: citric acid cycle
- pentose phosphate
- glycoproteins
- glycosaminoglycans
- phospholipid
- cholesterol and steroid
- sphingolipids
- eicosanoids
- amino acid
- urea cycle
- nucleotide
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| Disorders |
- Citric acid cycle and electron transport chain
- Glycoprotein
- Proteoglycan
- Fatty-acid
- Phospholipid
- Cholesterol and steroid
- Eicosanoid
- Amino acid
- Purine-pyrimidine
- Heme metabolism
- Symptoms and signs
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| Treatment | |
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| Carbohydrate metabolism | |
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| Primarily nervous system | |
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| Myopathies | |
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| No primary system | |
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| Chromosomal | |
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| see also mitochondrial proteins
Index of cells |
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| Description |
- Structure
- Organelles
- peroxisome
- cytoskeleton
- centrosome
- epithelia
- cilia
- mitochondria
- Membranes
- Membrane transport
- ion channels
- vesicular transport
- solute carrier
- ABC transporters
- ATPase
- oxidoreduction-driven
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| Disease |
- Structural
- peroxisome
- cytoskeleton
- cilia
- mitochondria
- nucleus
- scleroprotein
- Membrane
- channelopathy
- solute carrier
- ATPase
- ABC transporters
- other
- extracellular ligands
- cell surface receptors
- intracellular signalling
- Vesicular transport
- Pore-forming toxins
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