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Results 1 - 10 of 14 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. 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
  3. 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
  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. 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
  6. 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
  7. 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
  8. 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
  9. SDHB gene 
    ... DHSB_HUMAN FLJ92337 IP iron-sulfur subunit of complex II PGL4 SDH SDH1 SDH2 SDHIP succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial precursor ...
    https://medlineplus.gov/genetics/gene/sdhb - Genetics
  10. Multiple mitochondrial dysfunctions syndrome 
    ... function, including protein complexes called complex I, complex II, and complex III.Fe-S clusters are also required for another mitochondrial protein to function; this protein is involved in ...
    https://medlineplus.gov/...tiple-mitochondrial-dysfunctions-syndrome - Genetics
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