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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:Progressive Muscular Dystrophy, Pectorodorsal
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Accession:DOID:9000287 term browser browse the term
Synonyms:exact_synonym: Muscular Dystrophy, Progressive, Involving Shoulder Girdle and Back
 primary_id: MESH:C564095
 alt_id: OMIM:310095;   RDO:0013168



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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 40760
    Developmental Disease 36035
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 33173
        genetic disease 32754
          monogenic disease 18191
            X-linked monogenic disease 2075
              Progressive Muscular Dystrophy, Pectorodorsal 0
Path 2
Term Annotations click to browse term
  disease 40760
    disease of anatomical entity 32068
      nervous system disease 25939
        peripheral nervous system disease 5330
          neuropathy 5078
            neuromuscular disease 4022
              muscular disease 2788
                muscle tissue disease 1704
                  myopathy 1379
                    muscular dystrophy 838
                      Progressive Muscular Dystrophy, Pectorodorsal 0
paths to the root