Myositis

Symptom Information:

Symptom ID: HPO:0100614
Synonyms:
Inflammatory disorder of muscle (disorder) [Orphanet:44550]
Myositis (disorder) [Orphanet:44550]
Myositis [Orphanet:44550]
Myositis [OMIM:Myositis]
Myositis [MedDRA:10028653]
Interstitial myositis [MedDRA:10028653]
Muscle inflammation [MedDRA:10028653]
Myalgia and myositis, unspecified [MedDRA:10028653]
Traumatic myositis ossificans [MedDRA:10028653]
Granulomatous myositis [MedDRA:10028653]
Myotenositis [MedDRA:10028653]
Quality:
Cross references:
Orphanet:44550 "Myositis" [Orphanet:44550]
OMIM: "Myositis" [OMIM:Myositis]
UMLS:C0027121 "Myositis" [Orphanet:44550]
Is a (Direct Parents):
Orphanet Muscle anomalies
HPO         Abnormality of muscle morphology
MedDRA Muscle infections and inflammations
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)
Database Frequency: 21 / 7739
Resource:

All diseases associated with this symptom:

Antisynthetase syndrome (Orphanet:81)
Beh├žet 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)