Myositis
Symptom Information:
Symptom ID: | HPO:0100614 | |||||||||||
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 musculature(HPO:0003011) Abnormality of muscle morphology(HPO:0011805) Myositis(HPO:0100614) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Muscle disorders(MedDRA:10028302) Muscle infections and inflammations(MedDRA:10021992) Myositis(HPO:0100614) |
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Database Frequency: | 21 / 7739 | |||||||||||
Resource: |
All diseases associated with this symptom:
Antisynthetase syndrome | (Orphanet:81) |
Behçet disease | (Orphanet:117) |
CREST syndrome | (Orphanet:90290) |
Cogan syndrome | (Orphanet:1467) |
Eosinophilic fasciitis | (Orphanet:3165) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Focal myositis | (Orphanet:48918) |
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE WITH OR WITHOUTFRONTOTEMPORAL DEMENTIA 2 | (OMIM:615422) |
Mixed connective tissue disease | (Orphanet:809) |
Pediatric systemic lupus erythematosus | (Orphanet:93552) |
Polyarteritis nodosa | (Orphanet:767) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Pyoderma gangrenosum | (Orphanet:48104) |
Pyogenic arthritis - pyoderma gangrenosum - acne | (Orphanet:69126) |
Pyomyositis | (Orphanet:764) |
STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET | (OMIM:615934) |
Scleroderma | (Orphanet:801) |
Systemic sclerosis | (Orphanet:90291) |
TRAPS syndrome | (Orphanet:32960) |
Thymoma | (Orphanet:99867) |
Whipple disease | (Orphanet:3452) |