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Results 1 - 10 of 12 for Mitochondrial complex III deficiency
  1. Mitochondrial complex III deficiency 
    Mitochondrial complex III deficiency is a genetic condition that can affect several parts of the body, including the brain, kidneys, ... for movement (skeletal muscles). Signs and symptoms of mitochondrial complex III deficiency usually begin in infancy but can appear later. ...
    https://medlineplus.gov/.../mitochondrial-complex-iii-deficiency - Genetics
  2. MT-CYB gene 
    ... Mutations in the MT-CYB gene can cause mitochondrial complex III deficiency. When caused by mutations in this gene, the ... brain.Most MT-CYB gene mutations that cause mitochondrial complex III deficiency change single protein building blocks (amino acids) in ...
    https://medlineplus.gov/genetics/gene/mt-cyb - Genetics
  3. BCS1L gene 
    ... with this condition. More About This Health Condition Mitochondrial complex III deficiency can be caused by BCS1L gene mutations. When ... from complex I. In addition, in BCS1L-related mitochondrial complex III deficiency, cells contain more mitochondria than normal, probably to ...
    https://medlineplus.gov/genetics/gene/bcs1l - Genetics
  4. Mitochondrial DNA 
    ... CYB gene found in mitochondrial DNA can cause mitochondrial complex III deficiency. When caused by mutations in this gene, the ... phosphorylation. Most MT-CYB gene mutations involved in mitochondrial complex III deficiency change single amino acids in the cytochrome b ...
    https://medlineplus.gov/genetics/chromosome/mitochondrial-dna - Genetics
  5. Mitochondrial Diseases (National Library of Medicine)  
    Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Chemicals in your digestive ...
    https://medlineplus.gov/mitochondrialdiseases.html - Health Topics
  6. Genetic Brain Disorders (National Library of Medicine)  
    A genetic brain disorder is caused by a variation or a mutation in a gene. A variation is a different form of a gene. A mutation is a change in a gene. ...
    https://medlineplus.gov/geneticbraindisorders.html - Health Topics
  7. GRACILE syndrome 
    ... J, van Coster R, Fellman V. Characterization of complex III deficiency and liver dysfunction in GRACILE syndrome caused by ...
    https://medlineplus.gov/genetics/condition/gracile-syndrome - Genetics
  8. Leigh syndrome 
    ... ClinicalTrials.gov NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 5; MC4DN5 LEIGH SYNDROME; LS PubMed ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
  9. BOLA3 gene 
    ... is characterized by impairment of more than one mitochondrial function, such as reduced activity of complex I, II, or III, pyruvate dehydrogenase, alpha-ketoglutarate dehydrogenase, or the glycine ...
    https://medlineplus.gov/genetics/gene/bola3 - Genetics
  10. NFU1 gene 
    ... is characterized by impairment of more than one mitochondrial function, such as reduced activity of complex I, II, or III, pyruvate dehydrogenase, alpha-ketoglutarate dehydrogenase, or the glycine ...
    https://medlineplus.gov/genetics/gene/nfu1 - Genetics
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