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ONTOLOGY REPORT - ANNOTATIONS


Term:Mitochondrial Complex I Deficiency, Nuclear Type 16
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Accession:DOID:9009270 term browser browse the term
Synonyms:exact_synonym: MC1DN16
 primary_id: OMIM:618238
For additional species annotation, visit the Alliance of Genome Resources.


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Mitochondrial Complex I Deficiency, Nuclear Type 16 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ndufaf5 NADH:ubiquinone oxidoreductase complex assembly factor 5 JBrowse link 3 133,232,412 133,261,932 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15489
    Nutritional and Metabolic Diseases 4374
      disease of metabolism 4374
        mitochondrial metabolism disease 310
          mitochondrial complex I deficiency 57
            Mitochondrial Complex I Deficiency, Nuclear Type 16 1
Path 2
Term Annotations click to browse term
  disease 0
    Developmental Diseases 8822
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7612
        genetic disease 7095
          inherited metabolic disorder 1887
            mitochondrial metabolism disease 310
              mitochondrial complex I deficiency 57
                Mitochondrial Complex I Deficiency, Nuclear Type 16 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.