Arthritis
Symptom Information:
Symptom ID: | HPO:0001369 | |||||||||||||||||||||||||
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) Arthritis(HPO:0001369) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Joint disorders(MedDRA:10023213) Arthropathies NEC(MedDRA:10003284) Arthritis(HPO:0001369) |
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Database Frequency: | 44 / 7739 | |||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET | (OMIM:615952) |
Alkaptonuria | (Orphanet:56) |
Behçet 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) |