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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:Brachial Palsy, Familial Congenital
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Accession:DOID:9005159 term browser browse the term
Synonyms:primary_id: MESH:C563901;   RDO:0013035
 alt_id: MIM:608585


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Term paths to the root
Path 1
Term Annotations click to browse term
  disease 19145
    disease of anatomical entity 18457
      nervous system disease 14363
        peripheral nervous system disease 4406
          neuropathy 4192
            brachial plexus neuropathy 1
              Brachial Palsy, Familial Congenital 0
paths to the root