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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:polyclonal hypergammaglobulinemia
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Accession:DOID:2344 term browser browse the term
Synonyms:xref: ICD10CM:D89.0;   ICD9CM:273.0;   NCI:C35885
For additional species annotation, visit the Alliance of Genome Resources.


show annotations for term's descendants           Sort by:
polyclonal hypergammaglobulinemia term browser
Symbol Object Name Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Copg1 COPI coat complex subunit gamma 1 ISS MouseDO NCBI chr 4:120,366,540...120,392,502
Ensembl chr 4:120,366,542...120,415,616 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 18969
    Nutritional and Metabolic Diseases 8246
      disease of metabolism 8246
        inherited metabolic disorder 6256
          plasma protein metabolism disease 10
            polyclonal hypergammaglobulinemia 1
Path 2
Term Annotations click to browse term
  disease 18969
    Developmental Disease 14401
      Congenital, Hereditary, and Neonatal Diseases and Abnormalities 13418
        genetic disease 13036
          inherited metabolic disorder 6256
            plasma protein metabolism disease 10
              polyclonal hypergammaglobulinemia 1
paths to the root