Elevated erythrocyte sedimentation rate

Symptom Information:

Symptom ID: HPO:0003565
Synonyms:
Elevated sedimentation rate [HPO:0003565]
High erythrocyte sedimentation rate [HPO:0003565]
Increased erythrocyte sedimentation rate [HPO:0003565]
Raised erythrocyte sedimentation rate [HPO:0003565]
Increased erythrocyte sedimentation rate [Orphanet:54770]
Erythrocyte sedimentation rate (ESR) raised (finding) [Orphanet:54770]
ESR raised [Orphanet:54770]
Elevated erythrocyte sedimentation rate [OMIM:Elevated erythrocyte sedimentation rate]
Elevated sedimentation rate [OMIM:Elevated sedimentation rate]
High erythrocyte sedimentation rate [OMIM:High erythrocyte sedimentation rate]
Increased erythrocyte sedimentation rate [OMIM:Increased erythrocyte sedimentation rate]
Raised erythrocyte sedimentation rate [OMIM:Raised erythrocyte sedimentation rate]
Biological inflammatory syndrome/increased erythrocyte sedimentation rate/CRP [Orphanet:54770]
Red blood cell sedimentation rate increased [Orphanet:54770]
Red blood cell sedimentation rate increased [MedDRA:10049187]
Blood sedimentation increased [MedDRA:10049187]
Elevated sedimentation rate [MedDRA:10049187]
Erythrocyte sedimentation incr [MedDRA:10049187]
Erythrocyte sedimentation increased [MedDRA:10049187]
Erythrocyte sedimentation rate high [MedDRA:10049187]
Erythrocyte sedimentation rate incr [MedDRA:10049187]
Erythrocyte sedimentation rate increased [MedDRA:10049187]
Erythrocytes sedimentation rate increased [MedDRA:10049187]
ESR increased [MedDRA:10049187]
ESR raised [MedDRA:10049187]
Raised ESR [MedDRA:10049187]
RBC sedimentation increased [MedDRA:10049187]
RBC sedimentation rate increased [MedDRA:10049187]
Sedimendation rate erythrocytes increased [MedDRA:10049187]
Sedimentation rate increased [MedDRA:10049187]
Elevated erythrocyte sedimentation rate (ESR) [OMIM:Elevated erythrocyte sedimentation rate (ESR)]
Elevated erythrocyte sedimentation rate (mean 90mm/h) [OMIM:Elevated erythrocyte sedimentation rate (mean 90mm/h)]
Increased erythrocyte sedimentation rate (ESR) [OMIM:Increased erythrocyte sedimentation rate (ESR)]
Raised ESR [OMIM:Raised ESR]
Biological inflammatory syndrome [Orphanet:54770]
Quality:
Cross references:
Orphanet:54770 "Biological inflammatory syndrome/increased erythrocyte sedimentation rate/CRP" [Orphanet:54770]
OMIM: "Elevated erythrocyte sedimentation rate" [OMIM:Elevated erythrocyte sedimentation rate]
OMIM: "Elevated sedimentation rate" [OMIM:Elevated sedimentation rate]
OMIM: "High erythrocyte sedimentation rate" [OMIM:High erythrocyte sedimentation rate]
OMIM: "Increased erythrocyte sedimentation rate" [OMIM:Increased erythrocyte sedimentation rate]
OMIM: "Raised erythrocyte sedimentation rate" [OMIM:Raised erythrocyte sedimentation rate]
OMIM: "Elevated erythrocyte sedimentation rate (ESR)" [OMIM:Elevated erythrocyte sedimentation rate (ESR)]
OMIM: "Elevated erythrocyte sedimentation rate (mean 90mm/h)" [OMIM:Elevated erythrocyte sedimentation rate (mean 90mm/h)]
OMIM: "Increased erythrocyte sedimentation rate (ESR)" [OMIM:Increased erythrocyte sedimentation rate (ESR)]
OMIM: "Raised ESR" [OMIM:Raised ESR]
UMLS:C0151632 "ESR raised" [Orphanet:54770]
Is a (Direct Parents):
HPO         Abnormality of metabolism/homeostasis
MedDRA Haematological analyses NEC
Orphanet Health status anomalies
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of metabolism/homeostasis(HPO:0001939)
          Elevated erythrocyte sedimentation rate(HPO:0003565)
MedDRA:
Investigations(MedDRA:10022891)
    Haematology investigations (incl blood groups)(MedDRA:10018851)
       Haematological analyses NEC(MedDRA:10018846)
          Elevated erythrocyte sedimentation rate(HPO:0003565)
Database Frequency: 31 / 7739
Resource:

All diseases associated with this symptom:

Autosomal recessive lymphoproliferative disease (Orphanet:238505)
CANDLE syndrome (Orphanet:325004)
Carney complex (Orphanet:1359)
Cerebroretinal vasculopathy (Orphanet:3421)
Cryptogenic organizing pneumonia (Orphanet:1302)
Desquamative interstitial pneumonia (Orphanet:98852)
FAMILIAL MEDITERRANEAN FEVER (OMIM:249100)
Fabry disease (Orphanet:324)
Giant cell arteritis (Orphanet:397)
HERNS syndrome (Orphanet:63261)
HYPERIMMUNOGLOBULIN G1(A1) SYNDROMEIMMUNOGLOBULIN HEAVY CHAIN REGULATOR, INCLUDED (OMIM:144120)
Hereditary vascular retinopathy (Orphanet:71291)
Hyperimmunoglobulinemia D with periodic fever (Orphanet:343)
Idiopathic recurrent pericarditis (Orphanet:251307)
JMP syndrome (Orphanet:324999)
Kawasaki disease (Orphanet:2331)
LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA (OMIM:608809)
LYMPHOPROLIFERATIVE SYNDROME 1 (OMIM:613011)
Muckle-Wells syndrome (Orphanet:575)
Nakajo-Nishimura syndrome (Orphanet:2615)
Polyarteritis nodosa, childhood-onset (OMIM:615688)
Proteasome disability syndrome (Orphanet:324977)
Retinal vasculopathy and cerebral leukodystrophy (Orphanet:247691)
SARCOIDOSIS, SUSCEPTIBILITY TO, 1 (OMIM:181000)
STING-ASSOCIATED VASCULOPATHY, INFANTILE-ONSET (OMIM:615934)
Sarcoidosis (Orphanet:797)
Sneddon syndrome (Orphanet:820)
TRAPS syndrome (Orphanet:32960)
Uhl anomaly (Orphanet:3403)
WISKOTT-ALDRICH SYNDROME (OMIM:301000)
WISKOTT-ALDRICH SYNDROME, AUTOSOMAL DOMINANT FORM (OMIM:600903)