Synovitis
Symptom Information:
Symptom ID: | HPO:0100769 | |||||||||||||||||||||||||||||
Synonyms: |
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Quality: | ||||||||||||||||||||||||||||||
Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |