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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 14860
    disease of anatomical entity 14527
      musculoskeletal system disease 6757
        muscular disease 1434
          Rhabdomyolysis 25
            myoglobinuria 6
              Myoglobinuria, Autosomal Dominant 0
Path 2
Term Annotations click to browse term
  disease 14860
    disease of anatomical entity 14527
      nervous system disease 12337
        peripheral nervous system disease 2985
          neuropathy 2786
            neuromuscular disease 2193
              muscular disease 1434
                muscle tissue disease 936
                  myopathy 765
                    myoglobinuria 6
                      Myoglobinuria, Autosomal Dominant 0
paths to the root