Statements (22)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
MeSH Unique Identifier
|
| https://www.w3.org/2000/01/rdf-schema#label |
D015470
|
| gptkbp:MeSH_ID |
gptkb:Rheumatoid_Arthritis
Diseases [C] Arthritis [C20.111.555] Arthritis, Rheumatoid Arthritis, Rheumatoid [C17.800.838.500] Autoimmune Diseases [C17.800] Autoimmune Diseases, Musculoskeletal [C17.800.838] Musculoskeletal Diseases [C20] RA (Rheumatoid Arthritis) Rheumatic Diseases [C20.111] |
| gptkbp:scopeNote |
A chronic systemic disease primarily of the joints, marked by inflammatory changes in the synovial membranes and articular structures, widespread fibrinoid degeneration of the collagen fibers in mesenchymal tissues, and by atrophy and rarefaction of bony structures. The cause is unknown, but autoimmune mechanisms have been implicated.
|
| gptkbp:seeAlso |
Caplan Syndrome
Felty Syndrome Juvenile Arthritis |
| gptkbp:species |
C17.800.838.500
C20.111.555.500 |
| gptkbp:bfsParent |
gptkb:acute_erythroid_leukemia
gptkb:acute_myelomonocytic_leukemia gptkb:acute_promyelocytic_leukemia |
| gptkbp:bfsLayer |
6
|