Synovitis

Symptom Information:

Symptom ID: HPO:0100769
Synonyms:
Synovitis (disorder) [Orphanet:46160]
Synovitis [Orphanet:46160]
Arthritis/synovitis/synovial proliferation [Orphanet:46160]
Synovitis [MedDRA:10042868]
Synovitis of elbow [MedDRA:10042868]
Synovitis of knee [MedDRA:10042868]
Synovitis of shoulder [MedDRA:10042868]
Synovitis villonodular [MedDRA:10042868]
Synovitis wrists &
feet [MedDRA:10042868]
Villonodular synovitis [MedDRA:10042868]
Villonodular synovitis involving ankle and foot [MedDRA:10042868]
Villonodular synovitis involving forearm [MedDRA:10042868]
Villonodular synovitis involving hand [MedDRA:10042868]
Villonodular synovitis involving lower leg [MedDRA:10042868]
Villonodular synovitis involving multiple sites [MedDRA:10042868]
Villonodular synovitis involving other specified sites [MedDRA:10042868]
Villonodular synovitis involving pelvic region and thigh [MedDRA:10042868]
Villonodular synovitis involving shoulder region [MedDRA:10042868]
Villonodular synovitis involving upper arm [MedDRA:10042868]
Villonodular synovitis, site unspecified [MedDRA:10042868]
Synovitis chronic [MedDRA:10042868]
Brodie's disease [MedDRA:10042868]
Hypertrophic synovitis [MedDRA:10042868]
Toxic synovitis [MedDRA:10042868]
Acute synovitis [MedDRA:10042868]
Synovitis wrist [MedDRA:10042868]
Synovitis ankle [MedDRA:10042868]
Synovitis hip [MedDRA:10042868]
Quality:
Cross references:
Orphanet:46160 "Arthritis/synovitis/synovial proliferation" [Orphanet:46160]
UMLS:C0039103 "Synovitis" [Orphanet:46160]
Is a (Direct Parents):
Orphanet Abnormal cartilage morphology
MedDRA Synovial disorders
HPO         Abnormality of the synovia
Orphanet Arthritis
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)
                Abnormality of the synovia(HPO:0005262)
                   Synovitis(HPO:0100769)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Synovial and bursal disorders(MedDRA:10013361)
       Synovial disorders(MedDRA:10013360)
          Synovitis(HPO:0100769)
Database Frequency: 86 / 7739
Resource:

All diseases associated with this symptom:

22q11.2 deletion syndrome (Orphanet:567)
Adiposis dolorosa (Orphanet:36397)
Adult Still's disease (Orphanet:829)
Albers-Schönberg osteopetrosis (Orphanet:53)
Alkaptonuria (Orphanet:56)
Alpha-mannosidosis (Orphanet:61)
Angel-shaped phalango-epiphyseal dysplasia (Orphanet:63442)
Anti-glomerular basement membrane disease (Orphanet:375)
Aspartylglucosaminuria (Orphanet:93)
Autosomal agammaglobulinemia (Orphanet:33110)
Behçet disease (Orphanet:117)
Blau syndrome (Orphanet:90340)
Brachydactylous dwarfism, Mseleni type (Orphanet:2619)
Buschke-Ollendorff syndrome (Orphanet:1306)
CINCA syndrome (Orphanet:1451)
Castleman disease (Orphanet:160)
Chronic recurrent multifocal osteomyelitis (Orphanet:324964)
Congenital atransferrinemia (Orphanet:1195)
Cranio-osteoarthropathy (Orphanet:1525)
Cryoglobulinemic vasculitis (Orphanet:91138)
Dermatomyositis (Orphanet:221)
Diffuse cutaneous systemic sclerosis (Orphanet:220393)
Dracunculiasis (Orphanet:231)
Ehlers-Danlos syndrome, hypermobility type (Orphanet:285)
Eng-Strom syndrome (Orphanet:1937)
Enthesitis-related arthritis (Orphanet:85438)
Eosinophilic fasciitis (Orphanet:3165)
Eosinophilic granulomatosis with polyangiitis (Orphanet:183)
Fabry disease (Orphanet:324)
Familial Mediterranean fever (Orphanet:342)
Familial articular chondrocalcinosis (Orphanet:1416)
Familial cold urticaria (Orphanet:47045)
Felty syndrome (Orphanet:47612)
Giant cell arteritis (Orphanet:397)
Haim-Munk syndrome (Orphanet:2342)
Hyperimmunoglobulinemia D with periodic fever (Orphanet:343)
Hypocomplementemic urticarial vasculitis (Orphanet:36412)
Immunoglobulin A vasculitis (Orphanet:761)
Isolated agammaglobulinemia (Orphanet:229717)
Juvenile dermatomyositis (Orphanet:93672)
Juvenile idiopathic arthritis (Orphanet:92)
Juvenile rheumatoid factor-negative polyarthritis (Orphanet:85408)
Juvenile rheumatoid factor-positive polyarthritis (Orphanet:85435)
KID syndrome (Orphanet:477)
Kawasaki disease (Orphanet:2331)
Lesch-Nyhan syndrome (Orphanet:510)
Limited systemic sclerosis (Orphanet:220407)
Lyme disease (Orphanet:91546)
Majeed syndrome (Orphanet:77297)
Marshall syndrome with periodic fever (Orphanet:42642)
Melorheostosis (Orphanet:2485)
Microscopic polyangiitis (Orphanet:727)
Mixed connective tissue disease (Orphanet:809)
Muckle-Wells syndrome (Orphanet:575)
Multicentric reticulohistiocytosis (Orphanet:139436)
Multiple osteochondromas (Orphanet:321)
Myalgia-eosinophilia syndrome associated with tryptophan (Orphanet:2582)
Noonan syndrome (Orphanet:648)
Oculocerebrorenal syndrome (Orphanet:534)
Pachydermoperiostosis (Orphanet:2796)
Pediatric systemic sclerosis (Orphanet:93567)
Polyarteritis nodosa (Orphanet:767)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Polymyositis (Orphanet:732)
Pyogenic arthritis - pyoderma gangrenosum - acne (Orphanet:69126)
Rabson-Mendenhall syndrome (Orphanet:769)
Reactive arthritis (Orphanet:29207)
Relapsing polychondritis (Orphanet:728)
Renal cysts and diabetes syndrome (Orphanet:93111)
Reynolds syndrome (Orphanet:779)
Rheumatic fever (Orphanet:3099)
SAPHO syndrome (Orphanet:793)
Schnitzler syndrome (Orphanet:37748)
Scleroderma (Orphanet:801)
Secondary intestinal lymphangiectasia (Orphanet:90363)
Systemic sclerosis (Orphanet:90291)
Systemic-onset juvenile idiopathic arthritis (Orphanet:85414)
TRAPS syndrome (Orphanet:32960)
Takayasu arteritis (Orphanet:3287)
Talo-patello-scaphoid osteolysis (Orphanet:50809)
Thymoma (Orphanet:99867)
Torg-Winchester syndrome (Orphanet:3460)
Whipple disease (Orphanet:3452)
Wilson-Turner syndrome (Orphanet:3459)
Wiskott-Aldrich syndrome (Orphanet:906)
X-linked agammaglobulinemia (Orphanet:47)