Arthralgia/arthritis
Symptom Information:
Symptom ID: | HPO:0005059 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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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) Arthralgia(HPO:0002829) Arthralgia/arthritis(HPO:0005059) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Joint disorders(MedDRA:10023213) Arthropathies NEC(MedDRA:10003284) Arthralgia/arthritis(HPO:0005059) Joint related signs and symptoms(MedDRA:10023226) Arthralgia/arthritis(HPO:0005059) |
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Database Frequency: | 141 / 7739 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Acromegaly | (Orphanet:963) |
Acroosteolysis, dominant type | (Orphanet:955) |
Acute intermittent porphyria | (Orphanet:79276) |
Adiposis dolorosa | (Orphanet:36397) |
Adult Still's disease | (Orphanet:829) |
Aggressive systemic mastocytosis | (Orphanet:98850) |
Alkaptonuria | (Orphanet:56) |
Anti-glomerular basement membrane disease | (Orphanet:375) |
Arachnoiditis | (Orphanet:137817) |
Autoimmune hemolytic anemia, warm type | (Orphanet:90033) |
Babesiosis | (Orphanet:108) |
Behçet disease | (Orphanet:117) |
Beta-thalassemia major | (Orphanet:231214) |
Blau syndrome | (Orphanet:90340) |
Buerger disease | (Orphanet:36258) |
Buschke-Ollendorff syndrome | (Orphanet:1306) |
CINCA syndrome | (Orphanet:1451) |
Cardiomyopathy-cataract-hip spine disease | (Orphanet:1345) |
Carney complex | (Orphanet:1359) |
Cobb syndrome | (Orphanet:53721) |
Cogan syndrome | (Orphanet:1467) |
Cold agglutinin disease | (Orphanet:56425) |
Common variable immunodeficiency | (Orphanet:1572) |
Cranio-osteoarthropathy | (Orphanet:1525) |
Cryoglobulinemic vasculitis | (Orphanet:91138) |
Cutaneous leukocytoclastic angiitis | (Orphanet:889) |
Cutaneous lupus erythematosus | (Orphanet:535) |
Dengue fever | (Orphanet:99828) |
Dermatomyositis | (Orphanet:221) |
Dermatoosteolysis, Kirghizian type | (Orphanet:1657) |
Desmoid tumor | (Orphanet:873) |
Ehlers-Danlos syndrome due to tenascin-X deficiency | (Orphanet:230839) |
Ehlers-Danlos syndrome, hypermobility type | (Orphanet:285) |
Eosinophilic fasciitis | (Orphanet:3165) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Erythema elevatum diutinum | (Orphanet:90000) |
Fabry disease | (Orphanet:324) |
Familial Mediterranean fever | (Orphanet:342) |
Familial articular chondrocalcinosis | (Orphanet:1416) |
Familial cold urticaria | (Orphanet:47045) |
Familial symmetric lipomatosis | (Orphanet:2398) |
Farber lipogranulomatosis | (Orphanet:333) |
Felty syndrome | (Orphanet:47612) |
GM1 gangliosidosis | (Orphanet:354) |
Gaucher disease | (Orphanet:355) |
Gaucher disease type 1 | (Orphanet:77259) |
Giant cell arteritis | (Orphanet:397) |
Granulomatosis with polyangiitis | (Orphanet:900) |
Hemochromatosis type 2 | (Orphanet:79230) |
Hemochromatosis type 4 | (Orphanet:139491) |
Hemorrhagic fever - renal syndrome | (Orphanet:340) |
Hereditary coproporphyria | (Orphanet:79273) |
Hutchinson-Gilford progeria syndrome | (Orphanet:740) |
Hyperimmunoglobulinemia D with periodic fever | (Orphanet:343) |
IgA NEPHROPATHY, SUSCEPTIBILITY TO, 1 | (OMIM:161950) |
IgA NEPHROPATHY, SUSCEPTIBILITY TO, 2 | (OMIM:613944) |
Immunoglobulin A vasculitis | (Orphanet:761) |
Juvenile dermatomyositis | (Orphanet:93672) |
Juvenile idiopathic arthritis | (Orphanet:92) |
Juvenile rheumatoid factor-negative polyarthritis | (Orphanet:85408) |
Juvenile rheumatoid factor-positive polyarthritis | (Orphanet:85435) |
Kawasaki disease | (Orphanet:2331) |
Kienbock disease | (Orphanet:97332) |
Kniest dysplasia | (Orphanet:485) |
Lassa fever | (Orphanet:99824) |
Ledderhose disease | (Orphanet:199251) |
Legg-Calvé-Perthes disease | (Orphanet:2380) |
Legionellosis | (Orphanet:549) |
Lowry-Wood syndrome | (Orphanet:1824) |
Lyme disease | (Orphanet:91546) |
Macrophagic myofasciitis | (Orphanet:592) |
Madelung deformity | (Orphanet:35688) |
Majeed syndrome | (Orphanet:77297) |
Mandibuloacral dysplasia | (Orphanet:2457) |
Mandibuloacral dysplasia with type A lipodystrophy | (Orphanet:90153) |
Marburg hemorrhagic fever | (Orphanet:99826) |
Marfan syndrome | (Orphanet:558) |
Marshall syndrome | (Orphanet:560) |
Marshall syndrome with periodic fever | (Orphanet:42642) |
Melorheostosis | (Orphanet:2485) |
Microscopic polyangiitis | (Orphanet:727) |
Mixed connective tissue disease | (Orphanet:809) |
Mixed-type autoimmune hemolytic anemia | (Orphanet:90036) |
Muckle-Wells syndrome | (Orphanet:575) |
Mucopolysaccharidosis type 1 | (Orphanet:579) |
Multiple epiphyseal dysplasia due to collagen 9 anomaly | (Orphanet:166002) |
Multiple epiphyseal dysplasia type 1 | (Orphanet:93308) |
Multiple epiphyseal dysplasia type 4 | (Orphanet:93307) |
Multiple epiphyseal dysplasia type 5 | (Orphanet:93311) |
Multiple epiphyseal dysplasia, with severe proximal femoral dysplasia | (Orphanet:166029) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Nasu-Hakola disease | (Orphanet:2770) |
Necrotizing encephalomyelopathy, subacute, of Leigh, adult | (OMIM:161700) |
Neuralgic amyotrophy | (Orphanet:2901) |
Neurogenic thoracic outlet syndrome | (Orphanet:100073) |
Nodular non-suppurative panniculitis | (Orphanet:33577) |
Oligoarticular juvenile arthritis | (Orphanet:85410) |
Otospondylomegaepiphyseal dysplasia | (Orphanet:1427) |
PSORIASIS 1, SUSCEPTIBILITY TO | (OMIM:177900) |
Pachydermoperiostosis | (Orphanet:2796) |
Paroxysmal cold hemoglobinuria | (Orphanet:90035) |
Partial acquired lipodystrophy | (Orphanet:79087) |
Polyarteritis nodosa | (Orphanet:767) |
Polycythemia vera | (Orphanet:729) |
Polymyositis | (Orphanet:732) |
Primary familial polycythemia | (Orphanet:90042) |
Pseudoachondroplasia | (Orphanet:750) |
Pyogenic arthritis - pyoderma gangrenosum - acne | (Orphanet:69126) |
Reactive arthritis | (Orphanet:29207) |
Relapsing polychondritis | (Orphanet:728) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Rheumatic fever | (Orphanet:3099) |
Rift valley fever | (Orphanet:319251) |
SPONDYLOARTHROPATHY, SUSCEPTIBILITY TO, 1 | (OMIM:106300) |
Schnitzler syndrome | (Orphanet:37748) |
Scleroderma | (Orphanet:801) |
Spondyloepimetaphyseal dysplasia, Irapa type | (Orphanet:93351) |
Spondyloepiphyseal dysplasia tarda | (Orphanet:93284) |
Stickler syndrome | (Orphanet:828) |
Stickler syndrome type 1 | (Orphanet:90653) |
Stickler syndrome type 3 | (Orphanet:166100) |
Sweet syndrome | (Orphanet:3243) |
Systemic mastocytosis | (Orphanet:2467) |
Systemic sclerosis | (Orphanet:90291) |
Systemic-onset juvenile idiopathic arthritis | (Orphanet:85414) |
TRAPS syndrome | (Orphanet:32960) |
TRICHORHINOPHALANGEAL SYNDROME, TYPE I | (OMIM:190350) |
Takayasu arteritis | (Orphanet:3287) |
Thoracic outlet syndrome | (Orphanet:97330) |
Trochlear dysplasia | (Orphanet:1863) |
Typhoid | (Orphanet:99745) |
Ulna metaphyseal dysplasia syndrome | (Orphanet:1837) |
VITAMIN D-DEPENDENT RICKETS, TYPE 2B, WITH NORMAL VITAMIN D RECEPTOR | (OMIM:600785) |
Viral hemorrhagic fever | (Orphanet:341) |
WIDOW'S PEAK SYNDROME | (OMIM:314570) |
Whipple disease | (Orphanet:3452) |
Williams syndrome | (Orphanet:904) |
Wilson disease | (Orphanet:905) |
Wilson-Turner syndrome | (Orphanet:3459) |
Xeroderma pigmentosum | (Orphanet:910) |
Yellow fever | (Orphanet:99829) |