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RGD uses the Human Disease Ontology (DO, 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: OMIM:608585
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 16085
    disease of anatomical entity 15340
      nervous system disease 10967
        peripheral nervous system disease 2498
          neuropathy 2319
            brachial plexus neuropathy 1
              Brachial Palsy, Familial Congenital 0
paths to the root