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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:Congenital Muscular Dystrophy with Rapid Progression
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Accession:DOID:9003958 term browser browse the term
Synonyms:primary_id: MESH:C564983
 alt_id: OMIM:254100;   RDO:0013759
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 12006
    physical disorder 2318
      congenital muscular dystrophy 70
        Congenital Muscular Dystrophy with Rapid Progression 0
Path 2
Term Annotations click to browse term
  disease 12006
    disease of anatomical entity 11571
      nervous system disease 9482
        peripheral nervous system disease 2239
          neuropathy 2086
            neuromuscular disease 1641
              muscular disease 1080
                muscle tissue disease 732
                  myopathy 587
                    muscular dystrophy 291
                      congenital muscular dystrophy 70
                        Congenital Muscular Dystrophy with Rapid Progression 0
paths to the root