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Results 1 - 10 of 11 for Mitochondrial complex 1 "deficiency," nuclear type 9
  1. Cytochrome c oxidase deficiency 
    ... ClinicalTrials.gov MITOCHONDRIAL ... DEFICIENCY, NUCLEAR TYPE 9; MC4DN9 MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 13; ...
    https://medlineplus.gov/.../cytochrome-c-oxidase-deficiency - Genetics
  2. Mitochondrial complex III deficiency 
    ... Ubiquinone-cytochrome c oxidoreductase deficiency Genetic Testing Registry: Mitochondrial complex III deficiency nuclear type 1 Genetic Testing Registry: Mitochondrial complex III deficiency nuclear ...
    https://medlineplus.gov/.../mitochondrial-complex-iii-deficiency - Genetics
  3. Mitochondrial complex V deficiency 
    ... Rare Disorders (NORD) MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 1; MC5DN1 MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 4B; MC5DN4B ...
    https://medlineplus.gov/.../mitochondrial-complex-v-deficiency - Genetics
  4. Mitochondrial complex I deficiency 
    ... National Organization for Rare Disorders (NORD) ClinicalTrials.gov MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 1; MC1DN1 PubMed Alston CL, Rocha MC, Lax NZ, ...
    https://medlineplus.gov/.../mitochondrial-complex-i-deficiency - Genetics
  5. BCS1L gene 
    ... mitochondrial complex III assembly Tests of BCS1L PubMed MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 1; MC3DN1 BCS1 HOMOLOG, UBIQUINOL-CYTOCHROME C REDUCTASE COMPLEX ...
    https://medlineplus.gov/genetics/gene/bcs1l - Genetics
  6. ACAD9 deficiency 
    ... ACAD9 deficiency Genetic Testing Registry: Acyl-CoA dehydrogenase 9 deficiency Isolated complex I deficiency National Organization for Rare Disorders (NORD) MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20; MC1DN20 PubMed Aintablian HK, Narayanan V, Belnap ...
    https://medlineplus.gov/genetics/condition/acad9-deficiency - Genetics
  7. Leigh syndrome 
    ... gov NECROTIZING ENCEPHALOMYELOPATHY, SUBACUTE, OF LEIGH, ADULT ... S. Mitochondrial DNA-Associated Leigh Syndrome Spectrum. 2003 Oct 30 [updated 2024 May 9]. In: Adam MP, Feldman J, Mirzaa GM, Pagon ...
    https://medlineplus.gov/genetics/condition/leigh-syndrome - Genetics
  8. Combined oxidative phosphorylation deficiency 1 
    ... elongation factor G1 function. As a result, fewer mitochondrial proteins ... phosphorylation deficiency 1 because it impairs the function of more than ...
    https://medlineplus.gov/...ed-oxidative-phosphorylation-deficiency-1 - Genetics
  9. SDHA gene 
    ... SDH1 SDH2 SDHF succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial succinate dehydrogenase complex flavoprotein ... 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
  10. Parkinson's Disease From the National Institutes of Health (National Institute of Environmental Health Sciences)  
    Parkinson's Disease/Statistics and Research ... Parkinson's Disease ... National Institute of Environmental Health Sciences ... From the National Institutes of Health
    https://www.niehs.nih.gov/health/topics/conditions/parkinson - External Health Links
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