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ONTOLOGY REPORT - ANNOTATIONS


Term:Mitochondrial Complex I Deficiency, Nuclear Type 19
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Accession:DOID:9009263 term browser browse the term
Synonyms:exact_synonym: MC1DN19
 related_synonym: mitochondrial complex I deficiency, mitochondrial type 19
 primary_id: OMIM:618241
For additional species annotation, visit the Alliance of Genome Resources.


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Mitochondrial Complex I Deficiency, Nuclear Type 19 term browser
Symbol Object Name JBrowse Chr Start Stop Reference
G Foxred1 FAD-dependent oxidoreductase domain containing 1 JBrowse link 8 36,401,317 36,410,589 RGD:8554872
RGD:7240710

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 15502
    Nutritional and Metabolic Diseases 4392
      disease of metabolism 4392
        mitochondrial metabolism disease 314
          mitochondrial complex I deficiency 59
            Mitochondrial Complex I Deficiency, Nuclear Type 19 1
Path 2
Term Annotations click to browse term
  disease 15502
    Developmental Diseases 8872
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 7669
        genetic disease 7157
          inherited metabolic disorder 1895
            mitochondrial metabolism disease 314
              mitochondrial complex I deficiency 59
                Mitochondrial Complex I Deficiency, Nuclear Type 19 1
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.