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ONTOLOGY REPORT - ANNOTATIONS


Term:Mitochondrial Complex I Deficiency, Nuclear Type 33
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Accession:DOID:9009292 term browser browse the term
Synonyms:exact_synonym: MC1DN33
 primary_id: OMIM:618253
For additional species annotation, visit the Alliance of Genome Resources.


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Mitochondrial Complex I Deficiency, Nuclear Type 33 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ndufa6 NADH:ubiquinone oxidoreductase subunit A6 JBrowse link NW_004936718 60,797 67,614 RGD:7240710
RGD:9068941

Term paths to the root
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Term Annotations click to browse term
  disease 11547
    Nutritional and Metabolic Diseases 3185
      disease of metabolism 3185
        mitochondrial metabolism disease 297
          mitochondrial complex I deficiency 56
            Mitochondrial Complex I Deficiency, Nuclear Type 33 1
Path 2
Term Annotations click to browse term
  disease 11547
    Developmental Diseases 8114
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7058
        genetic disease 6596
          inherited metabolic disorder 1636
            mitochondrial metabolism disease 297
              mitochondrial complex I deficiency 56
                Mitochondrial Complex I Deficiency, Nuclear Type 33 1
paths to the root

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.