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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 22 41,066,111 41,074,852 RGD:9068941
RGD:7240710

Term paths to the root
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Term Annotations click to browse term
  disease 12058
    Nutritional and Metabolic Diseases 3268
      disease of metabolism 3268
        mitochondrial metabolism disease 296
          mitochondrial complex I deficiency 55
            Mitochondrial Complex I Deficiency, Nuclear Type 33 1
Path 2
Term Annotations click to browse term
  disease 12058
    Developmental Diseases 8433
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7284
        genetic disease 6809
          inherited metabolic disorder 1670
            mitochondrial metabolism disease 296
              mitochondrial complex I deficiency 55
                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.