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Results 1 - 10 of 17 for Mitochondrial complex II deficiency
  1. Mitochondrial complex I deficiency 
    ... Legrand A, Benit P, Rustin P, Slama A. Mitochondrial complex I deficiency of nuclear origin II. Non-structural genes. Mol Genet Metab. 2012 Feb; ...
    https://medlineplus.gov/.../mitochondrial-complex-i-deficiency - Genetics
  2. 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
  3. SDHA gene 
    ... Condition CMD1GG DHSA_HUMAN flavoprotein subunit of complex ... Belinsky MG, Rink L, von Mehren M. Succinate dehydrogenase deficiency in pediatric and adult gastrointestinal stromal tumors. Front ...
    https://medlineplus.gov/genetics/gene/sdha - Genetics
  4. 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
  5. SDHD gene 
    ... and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma. Cancer Res. 2000 Dec ...
    https://medlineplus.gov/genetics/gene/sdhd - Genetics
  6. 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
  7. 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
  8. 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 ...
    https://medlineplus.gov/genetics/gene/bola3 - Genetics
  9. 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 ...
    https://medlineplus.gov/genetics/gene/nfu1 - Genetics
  10. HSD10 disease 
    ... deficiency 3H2MBD deficiency HSD10 deficiency Hydroxyacyl-CoA dehydrogenase II deficiency MHBD deficiency Genetic Testing Registry: HSD10 mitochondrial disease HSD10 disease National Organization for Rare Disorders ( ...
    https://medlineplus.gov/genetics/condition/hsd10-disease - Genetics
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