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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 12822
    physical disorder 2385
      congenital muscular dystrophy 68
        Congenital Muscular Dystrophy with Rapid Progression 0
Path 2
Term Annotations click to browse term
  disease 12822
    disease of anatomical entity 12355
      nervous system disease 10079
        peripheral nervous system disease 2335
          neuropathy 2170
            neuromuscular disease 1710
              muscular disease 1130
                muscle tissue disease 760
                  myopathy 615
                    muscular dystrophy 293
                      congenital muscular dystrophy 68
                        Congenital Muscular Dystrophy with Rapid Progression 0
paths to the root