Elevated C-reactive protein level
Symptom Information:
Symptom ID: | HPO:0011227 | ||||||||||||||||
Synonyms: |
|
||||||||||||||||
Quality: | |||||||||||||||||
Cross references: |
|
||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of circulating protein level(HPO:0010876) Elevated C-reactive protein level(HPO:0011227) MedDRA: Investigations(MedDRA:10022891) Haematology investigations (incl blood groups)(MedDRA:10018851) Coagulation and bleeding analyses(MedDRA:10009728) Elevated C-reactive protein level(HPO:0011227) Protein and chemistry analyses NEC(MedDRA:10037000) Protein analyses NEC(MedDRA:10036998) Elevated C-reactive protein level(HPO:0011227) |
||||||||||||||||
Database Frequency: | 55 / 7739 | ||||||||||||||||
Resource: |
All diseases associated with this symptom:
Acute interstitial pneumonia | (Orphanet:79126) |
Adult Still's disease | (Orphanet:829) |
Alström syndrome | (Orphanet:64) |
Behçet disease | (Orphanet:117) |
Blau syndrome | (Orphanet:90340) |
CANDLE syndrome | (Orphanet:325004) |
CINCA syndrome | (Orphanet:1451) |
Camurati-Engelmann disease | (Orphanet:1328) |
Castleman disease | (Orphanet:160) |
Chronic recurrent multifocal osteomyelitis | (Orphanet:324964) |
Cogan syndrome | (Orphanet:1467) |
Common variable immunodeficiency | (Orphanet:1572) |
Cryptogenic organizing pneumonia | (Orphanet:1302) |
Dermatomyositis | (Orphanet:221) |
Enthesitis-related arthritis | (Orphanet:85438) |
Eosinophilic granulomatosis with polyangiitis | (Orphanet:183) |
Familial Mediterranean fever | (Orphanet:342) |
Gaucher disease | (Orphanet:355) |
Giant cell arteritis | (Orphanet:397) |
Granulomatosis with polyangiitis | (Orphanet:900) |
Hyperimmunoglobulinemia D with periodic fever | (Orphanet:343) |
Idiopathic acute eosinophilic pneumonia | (Orphanet:724) |
Idiopathic recurrent pericarditis | (Orphanet:251307) |
JMP syndrome | (Orphanet:324999) |
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) |
LYMPHOPROLIFERATIVE SYNDROME 1 | (OMIM:613011) |
Macrophagic myofasciitis | (Orphanet:592) |
Majeed syndrome | (Orphanet:77297) |
Marshall syndrome with periodic fever | (Orphanet:42642) |
Microscopic polyangiitis | (Orphanet:727) |
Mixed connective tissue disease | (Orphanet:809) |
Muckle-Wells syndrome | (Orphanet:575) |
Multiple endocrine neoplasia type 2 | (Orphanet:653) |
NLRP12-associated hereditary periodic fever syndrome | (Orphanet:247868) |
Nakajo-Nishimura syndrome | (Orphanet:2615) |
Oligoarticular juvenile arthritis | (Orphanet:85410) |
Polyarteritis nodosa | (Orphanet:767) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Proteasome disability syndrome | (Orphanet:324977) |
Purine nucleoside phosphorylase deficiency | (Orphanet:760) |
Pyogenic arthritis - pyoderma gangrenosum - acne | (Orphanet:69126) |
Pyomyositis | (Orphanet:764) |
Reactive arthritis | (Orphanet:29207) |
Relapsing polychondritis | (Orphanet:728) |
Rheumatic fever | (Orphanet:3099) |
SAPHO syndrome | (Orphanet:793) |
Sweet syndrome | (Orphanet:3243) |
Systemic-onset juvenile idiopathic arthritis | (Orphanet:85414) |
TRAPS syndrome | (Orphanet:32960) |
Takayasu arteritis | (Orphanet:3287) |
Waldenström macroglobulinemia | (Orphanet:33226) |