Elevated erythrocyte sedimentation rate
Symptom Information:
Symptom ID: | HPO:0003565 | |||||||||||||||||||||||||||||||||||
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 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) |
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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) |