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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:fibromyalgia
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Accession:DOID:631 term browser browse the term
Definition:A syndrome that is is characterized by chronic widespread musculoskeletal pain, fatigue, sleep disturbances, cognitive dysfunction and depression. (DO)
Synonyms:exact_synonym: Diffuse Myofascial Pain Syndrome;   Fibromyalgia Fibromyositis Syndrome;   Fibromyalgias;   Fibrositides;   Fibrositis;   Muscular Rheumatism;   Primary Fibromyalgia;   Primary Fibromyalgias;   Secondary Fibromyalgia;   fibromyalgia-fibromyositis syndromes;   secondary fibromyalgias
 primary_id: MESH:D005356
 xref: ICD10CM:M79.7;   NCI:C50566;   NCI:C87497
For additional species annotation, visit the Alliance of Genome Resources.


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fibromyalgia term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Cat catalase ISO protein:decreased activity:mononuclear cell: RGD PMID:22532869 RGD:9479066 NCBI chrNW_004936533:3,601,270...3,637,128 JBrowse link
G Comt catechol-O-methyltransferase severity ISO DNA:polymorphism:cds:p.V158M(human) RGD PMID:24762091 RGD:13450944 NCBI chrNW_004936619:3,847,059...3,883,866 JBrowse link
G Il1rn interleukin 1 receptor antagonist severity ISO protein:increased expression:serum (human) RGD PMID:10341365 RGD:8549787 NCBI chrNW_004936783:1,447,158...1,466,331 JBrowse link
erythema nodosum term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G C3 complement C3 ISO associated with Leprosy RGD PMID:2783924 RGD:7421527 NCBI chrNW_004936588:3,985,732...4,023,221 JBrowse link
G Cfb complement factor B ISO associated with Leprosy RGD PMID:2783924 RGD:7421527 NCBI chrNW_004936727:1,595,872...1,602,274 JBrowse link
G Lta lymphotoxin alpha ISO associated with Sarcoidosis;DNA:polymorphism:intron RGD PMID:19225544 RGD:8548773 NCBI chrNW_004936727:1,940,081...1,941,022 JBrowse link
G Tnf tumor necrosis factor susceptibility ISO associated with Inflammatory Bowel Diseases;DNA:polymorphisms: :-1031T>C(human) RGD PMID:12198697 RGD:7364926 NCBI chrNW_004936727:1,936,066...1,937,766 JBrowse link
G Vdr vitamin D receptor susceptibility ISO associated with Behcet Syndrome;DNA:polymorphism: : rs7975232(human) RGD PMID:24880677 RGD:13217417 NCBI chrNW_004936512:5,741,836...5,800,999 JBrowse link
otulipenia term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Otulin OTU deubiquitinase with linear linkage specificity ISO OMIM NCBI chrNW_004936665:1,654,045...1,690,955 JBrowse link
Subcutaneous Panniculitis-like T-Cell Lymphoma term browser
Symbol Object Name Qualifiers Evidence Notes Source PubMed Reference(s) RGD Reference(s) Position
G Havcr2 hepatitis A virus cellular receptor 2 ISO OMIM NCBI chrNW_004936515:6,001,324...6,015,407 JBrowse link

Term paths to the root
Path 1
Term Annotations click to browse term
  disease 13086
    disease of anatomical entity 12774
      musculoskeletal system disease 5642
        muscular disease 1193
          fibromyalgia 10
            panniculitis + 7
Path 2
Term Annotations click to browse term
  disease 13086
    disease of anatomical entity 12774
      nervous system disease 10565
        peripheral nervous system disease 2382
          neuropathy 2206
            neuromuscular disease 1753
              muscular disease 1193
                muscle tissue disease 765
                  myopathy 607
                    myositis 65
                      fibromyalgia 10
                        panniculitis + 7
paths to the root