Elevated C-reactive protein level

Symptom Information:

Symptom ID: HPO:0011227
Synonyms:
Elevated CRP [HPO:0011227]
Increased CRP serum level [Orphanet:54770]
Protein C increased [Orphanet:54770]
C-reactive protein increased [Orphanet:54770]
Biological inflammatory syndrome/increased erythrocyte sedimentation rate/CRP [Orphanet:54770]
Protein C increased [MedDRA:10060230]
Protein C antigen increased [MedDRA:10060230]
C-reactive protein increased [MedDRA:10006825]
C-reactive protein positive [MedDRA:10006825]
C-reactive protein result high [MedDRA:10006825]
CRP increased [MedDRA:10006825]
CRP positive [MedDRA:10006825]
High-sensitivity C-reactive protein increased [MedDRA:10006825]
hs-CRP increased [MedDRA:10006825]
Increased C-reactive protein [OMIM:Increased C-reactive protein]
Biological inflammatory syndrome [Orphanet:54770]
Quality:
Cross references:
Orphanet:54770 "Biological inflammatory syndrome/increased erythrocyte sedimentation rate/CRP" [Orphanet:54770]
OMIM: "Increased C-reactive protein" [OMIM:Increased C-reactive protein]
UMLS:C1168113 "Protein C increased" [Orphanet:54770]
UMLS:C0742906 "C-reactive protein increased" [Orphanet:54770]
Is a (Direct Parents):
HPO         Abnormality of circulating protein level
Orphanet Elevated erythrocyte sedimentation rate
MedDRA Coagulation and bleeding analyses
MedDRA Protein analyses NEC
Orphanet Health status anomalies
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)