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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:monoclonal gammopathy of uncertain significance
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Accession:DOID:7442 term browser browse the term
Definition:A blood protein disease that is characterized by the presence of an abnormal protein called monoclonal protein in the blood. (DO)
Synonyms:exact_synonym: Benign Monoclonal Gammopathies;   Benign Monoclonal Gammopathy;   MGUS;   monoclonal gammopathy;   monoclonal gammopathy of undetermined significance
 primary_id: MESH:D008998
 xref: EFO:0000203;   EFO:1000836;   GARD:7034;   NCI:C3996
For additional species annotation, visit the Alliance of Genome Resources.

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monoclonal gammopathy of uncertain significance term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Ctla4 cytotoxic T-lymphocyte associated protein 4 susceptibility ISO DNA:microsatellite polymorphism:exon: : RGD PMID:11167807 RGD:11352247 NCBI chrNW_004624765:12,449,205...12,454,324
Ensembl chrNW_004624765:12,449,205...12,454,324 		JBrowse link
G Myd88 MYD88 innate immune signal transduction adaptor ISO MouseDO NCBI chrNW_004624731:2,677,259...2,681,408
Ensembl chrNW_004624731:2,677,290...2,681,489 		JBrowse link
G Nefh neurofilament heavy chain ISO associated with Peripheral Nervous System Diseases RGD PMID:12536221 RGD:9693726 NCBI chrNW_004624747:5,806,576...5,816,158
Ensembl chrNW_004624747:5,806,645...5,815,554 		JBrowse link
Schnitzler syndrome term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Il1a interleukin 1 alpha ISO RGD PMID:1831824 RGD:7794711 NCBI chrNW_004624749:12,795,967...12,805,658
Ensembl chrNW_004624749:12,795,946...12,805,154 		JBrowse link
G Il1rn interleukin 1 receptor antagonist susceptibility ISO CTD Direct Evidence: therapeutic RGD
CTD		 PMID:16096327 RGD:11522758 NCBI chrNW_004624749:13,210,365...13,224,471
Ensembl chrNW_004624749:13,210,476...13,225,890 		JBrowse link
Term paths to the root
Path 1
Term Annotations click to browse term
  disease 14215
    Pathological Conditions, Signs and Symptoms 11244
      Signs and Symptoms 9457
        Hypergammaglobulinemia 17
          monoclonal gammopathy of uncertain significance 5
            Schnitzler syndrome 2
Path 2
Term Annotations click to browse term
  disease 14215
    disease of anatomical entity 13931
      Immune & Inflammatory Diseases 4784
        immune system disease 4249
          Immunoproliferative Disorders 999
            lymphoproliferative syndrome 993
              lymphoma 494
                non-Hodgkin lymphoma 420
                  B-cell lymphoma 309
                    mature B-cell neoplasm 175
                      plasma cell neoplasm 157
                        monoclonal gammopathy of uncertain significance 5
                          Schnitzler syndrome 2
paths to the root