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ONTOLOGY REPORT - ANNOTATIONS


Term:Mitochondrial Complex I Deficiency, Nuclear Type 18
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Accession:DOID:9009274 term browser browse the term
Synonyms:exact_synonym: MC1DN18
 primary_id: OMIM:618240
For additional species annotation, visit the Alliance of Genome Resources.


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Mitochondrial Complex I Deficiency, Nuclear Type 18 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Ndufaf3 NADH:ubiquinone oxidoreductase complex assembly factor 3 JBrowse link 8 117,351,628 117,353,460 RGD:8554872
RGD:7240710

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 18 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 18 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.