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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 15639
    Nutritional and Metabolic Diseases 4392
      disease of metabolism 4392
        mitochondrial metabolism disease 308
          mitochondrial complex I deficiency 57
            Mitochondrial Complex I Deficiency, Nuclear Type 16 1
Path 2
Term Annotations click to browse term
  disease 15639
    Developmental Diseases 8774
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7556
        genetic disease 7052
          inherited metabolic disorder 1879
            mitochondrial metabolism disease 308
              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.