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ONTOLOGY REPORT - ANNOTATIONS


Term:Mitochondrial Complex I Deficiency, Nuclear Type 2
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Accession:DOID:9003097 term browser browse the term
Synonyms:exact_synonym: MC1DN2
 primary_id: OMIM:618222
For additional species annotation, visit the Alliance of Genome Resources.


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Mitochondrial Complex I Deficiency, Nuclear Type 2 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ndufs8 NADH:ubiquinone oxidoreductase core subunit S8 JBrowse link 1 219,141,289 219,144,610 RGD:8554872
RGD:7240710

Term paths to the root
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Term Annotations click to browse term
  disease 15609
    Nutritional and Metabolic Diseases 4391
      disease of metabolism 4391
        mitochondrial metabolism disease 314
          mitochondrial complex I deficiency 60
            Mitochondrial Complex I Deficiency, Nuclear Type 2 1
Path 2
Term Annotations click to browse term
  disease 15609
    Developmental Diseases 8986
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7802
        genetic disease 7293
          inherited metabolic disorder 1909
            mitochondrial metabolism disease 314
              mitochondrial complex I deficiency 60
                Mitochondrial Complex I Deficiency, Nuclear Type 2 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.