Arthritis

Symptom Information:

Symptom ID: HPO:0001369
Synonyms:
Arthritis (disorder) [Orphanet:46160]
Arthritis [Orphanet:46160]
Arthritis [OMIM:Arthritis]
Arthritis/synovitis/synovial proliferation [Orphanet:46160]
Arthritis [MedDRA:10003246]
Arthritis aggravated [MedDRA:10003246]
Arthritis NOS [MedDRA:10003246]
Arthritis NOS aggravated [MedDRA:10003246]
Atrophic arthritis [MedDRA:10003246]
Flare up of arthritis [MedDRA:10003246]
Joint inflammation [MedDRA:10003246]
Joint swelling inflammatory [MedDRA:10003246]
Coxarthritis [MedDRA:10003246]
Gonarthritis [MedDRA:10003246]
Coxitis [MedDRA:10003246]
Arthritis flare up [MedDRA:10003246]
Omarthritis [MedDRA:10003246]
Finger arthritis [MedDRA:10003246]
Acute arthritis [MedDRA:10003246]
Chronic arthritis [MedDRA:10003246]
Knee arthritis [MedDRA:10003246]
Gonitis [MedDRA:10003246]
Pseudoseptic arthritis [MedDRA:10003246]
Arthritis (hip) [OMIM:Arthritis (hip)]
Arthritis (large joints, small joint, or central axial skeleton) [OMIM:Arthritis (large joints, small joint, or central axial skeleton)]
Quality:
Cross references:
HPO:0005059 "arthralgia/arthritis" [Orphanet:46160]
HPO:0002758 "Osteoarthritis" [Orphanet:46160]
Orphanet:46160 "Arthritis/synovitis/synovial proliferation" [Orphanet:46160]
OMIM: "Arthritis" [OMIM:Arthritis]
OMIM: "Arthritis (hip)" [OMIM:Arthritis (hip)]
OMIM: "Arthritis (large joints, small joint, or central axial skeleton)" [OMIM:Arthritis (large joints, small joint, or central axial skeleton)]
UMLS:C0003864 "Arthritis" [HPO:0001369]
UMLS:C0003864 "Arthritis" [Orphanet:46160]
Is a (Direct Parents):
HPO         Abnormal joint morphology
Orphanet Abnormal cartilage morphology
MedDRA Arthropathies NEC
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal joint morphology(HPO:0001367)
                Arthritis(HPO:0001369)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Joint disorders(MedDRA:10023213)
       Arthropathies NEC(MedDRA:10003284)
          Arthritis(HPO:0001369)
Database Frequency: 44 / 7739
Resource:

All diseases associated with this symptom:

AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET (OMIM:615952)
Alkaptonuria (Orphanet:56)
Beh├žet disease (Orphanet:117)
Blau syndrome (Orphanet:90340)
Buschke-Ollendorff syndrome (Orphanet:1306)
CAMPTODACTYLY-ARTHROPATHY-COXA VARA-PERICARDITIS SYNDROME (OMIM:208250)
COMPLEMENT COMPONENT C1r/C1s DEFICIENCY (OMIM:216950)
Cardiomyopathy-cataract-hip spine disease (Orphanet:1345)
Combined immunodeficiency with facio-oculo-skeletal anomalies (Orphanet:221139)
Congenital vertical talus (Orphanet:178382)
Cranio-osteoarthropathy (Orphanet:1525)
Diffuse cutaneous systemic sclerosis (Orphanet:220393)
FAMILIAL MEDITERRANEAN FEVER (OMIM:249100)
Familial Mediterranean fever (Orphanet:342)
Farber lipogranulomatosis (Orphanet:333)
Gaucher disease (Orphanet:355)
Gaucher disease type 1 (Orphanet:77259)
Hemochromatosis type 2 (Orphanet:79230)
Hemochromatosis type 3 (Orphanet:225123)
Hemochromatosis type 4 (Orphanet:139491)
Hyperimmunoglobulinemia D with periodic fever (Orphanet:343)
IMMUNODEFICIENCY, COMMON VARIABLE, 8, WITH AUTOIMMUNITY (OMIM:614700)
Immunodeficiency with factor I anomaly (Orphanet:200418)
Intestinal epithelial dysplasia (Orphanet:92050)
LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA (OMIM:608809)
Lesch-Nyhan syndrome (Orphanet:510)
Limited cutaneous systemic sclerosis (Orphanet:220402)
Mediterranean macrothrombocytopenia (Orphanet:101022)
Necrotizing encephalomyelopathy, subacute, of Leigh, adult (OMIM:161700)
PSORIASIS 1, SUSCEPTIBILITY TO (OMIM:177900)
Pediatric systemic lupus erythematosus (Orphanet:93552)
Pediatric systemic sclerosis (Orphanet:93567)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Pyogenic arthritis - pyoderma gangrenosum - acne (Orphanet:69126)
Renal cysts and diabetes syndrome (Orphanet:93111)
SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1 (OMIM:106300)
SYSTEMIC LUPUS ERYTHEMATOSUS (OMIM:152700)
Sarcoidosis (Orphanet:797)
Severe combined immunodeficiency due to complete RAG1/2 deficiency (Orphanet:331206)
Sitosterolemia (Orphanet:2882)
Spondyloepiphyseal dysplasia tarda (Orphanet:93284)
Wilson disease (Orphanet:905)
Wilson-Turner syndrome (Orphanet:3459)
[DEL] URIC ACID CONCENTRATION, SERUM, QUANTITATIVE TRAIT LOCUS 1 (OMIM:138900)