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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 5 6,562,074 6,567,321 RGD:7240710
RGD:9068941

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 12161
    Nutritional and Metabolic Diseases 3351
      disease of metabolism 3351
        mitochondrial metabolism disease 312
          mitochondrial complex I deficiency 60
            Mitochondrial Complex I Deficiency, Nuclear Type 33 1
Path 2
Term Annotations click to browse term
  disease 12161
    Developmental Diseases 8486
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7330
        genetic disease 6857
          inherited metabolic disorder 1700
            mitochondrial metabolism disease 312
              mitochondrial complex I deficiency 60
                Mitochondrial Complex I Deficiency, Nuclear Type 33 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.