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ONTOLOGY REPORT - ANNOTATIONS


Term:Mitochondrial Complex I Deficiency, Nuclear Type 8
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Accession:DOID:9005533 term browser browse the term
Synonyms:exact_synonym: MC1DN8
 primary_id: OMIM:618230
For additional species annotation, visit the Alliance of Genome Resources.


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Mitochondrial Complex I Deficiency, Nuclear Type 8 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ndufs3 NADH:ubiquinone oxidoreductase core subunit S3 JBrowse link 3 79,721,686 79,728,863 RGD:7240710
RGD:8554872

Term paths to the root
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Term Annotations click to browse term
  disease 15603
    Nutritional and Metabolic Diseases 4390
      disease of metabolism 4390
        mitochondrial metabolism disease 308
          mitochondrial complex I deficiency 57
            Mitochondrial Complex I Deficiency, Nuclear Type 8 1
Path 2
Term Annotations click to browse term
  disease 15603
    Developmental Diseases 8772
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7555
        genetic disease 7051
          inherited metabolic disorder 1877
            mitochondrial metabolism disease 308
              mitochondrial complex I deficiency 57
                Mitochondrial Complex I Deficiency, Nuclear Type 8 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.