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RGD DISEASE ONTOLOGY - ANNOTATIONS

RGD uses the Human Disease Ontology (DO, https://disease-ontology.org/) for disease curation across species. RGD automatically downloads each new release of the ontology on a monthly basis. Some additional terms which are required for RGD's curation purposes but are not currently covered in the official version of DO have been added. As corresponding terms are added to DO, these custom terms are retired and the DO terms substituted in existing annotations and subsequently used for curation.

Term:Myoglobinuria, Autosomal Dominant
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Accession:DOID:9007911 term browser browse the term
Synonyms:primary_id: MESH:C563546
 alt_id: OMIM:160010
For additional species annotation, visit the Alliance of Genome Resources.


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 13526
    disease of anatomical entity 13249
      musculoskeletal system disease 6312
        muscular disease 1348
          Rhabdomyolysis 24
            myoglobinuria 5
              Myoglobinuria, Autosomal Dominant 0
Path 2
Term Annotations click to browse term
  disease 13526
    disease of anatomical entity 13249
      nervous system disease 11298
        peripheral nervous system disease 2821
          neuropathy 2636
            neuromuscular disease 2066
              muscular disease 1348
                muscle tissue disease 879
                  myopathy 716
                    myoglobinuria 5
                      Myoglobinuria, Autosomal Dominant 0
paths to the root