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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:Felty's syndrome
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Accession:DOID:11042 term browser browse the term
Definition:A syndrome that results_in rheumatoid arthritis, splenomegaly and neutropenia. (DO)
Synonyms:exact_synonym: Familial Felty Syndrome;   Familial Feltys Syndrome;   Felty syndrome;   Feltys Syndrome;   familial Felty's syndrome;   rheumatoid arthritis with splenoadenomegaly and leukopenia;   rheumatoid arthritis, splenomegaly and neutropenia
 primary_id: MESH:D005258
 alt_id: OMIM:134750
 xref: EFO:0007269;   GARD:8234;   ICD10CM:M05.0;   ICD9CM:714.1;   NCI:C84712
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 21108
    syndrome 10708
      Felty's syndrome 0
Path 2
Term Annotations click to browse term
  disease 21108
    disease of anatomical entity 18147
      Immune & Inflammatory Diseases 5535
        immune system disease 4747
          primary immunodeficiency disease 4124
            autoimmune disease 2308
              autoimmune disease of musculoskeletal system 992
                rheumatic disease 779
                  rheumatoid arthritis 514
                    Felty's syndrome 0
paths to the root