Coenzyme Q10 deficiency

Classification	OMIM: 607426 614650 616276;
External resources	Orphanet: 255249;

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[edit | edit source]

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v t e Disorders of citric acid cycle and electron transport chain
Citric acid cycle	Pyruvate dehydrogenase deficiency Fumarase deficiency
Electron transport chain	Coenzyme Q10 deficiency Björnstad syndrome GRACILE syndrome Leigh's disease

v t e Mitochondrial diseases
Carbohydrate metabolism	PCD PDHA
Primarily nervous system	Leigh disease LHON NARP
Myopathies	KSS Mitochondrial encephalomyopathy MELAS MERRF PEO
No primary system	DAD MNGIE Pearson syndrome
Chromosomal	OPA1 Kjer's optic neuropathy SARS2 HUPRA syndrome TIMM8A Mohr–Tranebjærg syndrome
see also mitochondrial proteins

Classification	OMIM: 607426 614650 616276
External resources	Orphanet: 255249