Leukocytosis
Symptom Information:
Symptom ID: | HPO:0001974 | |||||||||||||||||||||
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 the immune system(HPO:0002715) Abnormality of cellular immune system(HPO:0010987) Abnormality of leukocytes(HPO:0001881) Abnormal leukocyte count(HPO:0011893) Leukocytosis(HPO:0001974) Abnormality of blood and blood-forming tissues(HPO:0001871) Abnormality of leukocytes(HPO:0001881) Abnormal leukocyte count(HPO:0011893) Leukocytosis(HPO:0001974) MedDRA: Investigations(MedDRA:10022891) Haematology investigations (incl blood groups)(MedDRA:10018851) White blood cell analyses(MedDRA:10047938) Leukocytosis(HPO:0001974) Blood and lymphatic system disorders(MedDRA:10005329) Abnormality of leukocytes(HPO:0001881) Leukocytoses NEC(MedDRA:10024379) Leukocytosis(HPO:0001974) |
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Database Frequency: | 33 / 7739 | |||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Adult Still's disease | (Orphanet:829) |
CINCA syndrome | (Orphanet:1451) |
Caffey disease | (Orphanet:1310) |
Cryptogenic organizing pneumonia | (Orphanet:1302) |
Cutis laxa | (Orphanet:209) |
Deafness - lymphedema - leukemia | (Orphanet:3226) |
FAMILIAL MEDITERRANEAN FEVER | (OMIM:249100) |
Familial cold urticaria | (Orphanet:47045) |
GRANULOCYTOPENIA WITH IMMUNOGLOBULIN ABNORMALITY | (OMIM:233600) |
Gaucher disease type 1 | (Orphanet:77259) |
Hairy cell leukemia variant | (Orphanet:300878) |
Hemorrhagic fever - renal syndrome | (Orphanet:340) |
Hyperimmunoglobulinemia D with periodic fever | (Orphanet:343) |
IVIC syndrome | (Orphanet:2307) |
Idiopathic recurrent pericarditis | (Orphanet:251307) |
Kawasaki disease | (Orphanet:2331) |
LIG4 syndrome | (Orphanet:99812) |
Leprechaunism | (Orphanet:508) |
Leukocyte adhesion deficiency | (Orphanet:2968) |
Leukocyte adhesion deficiency type III | (Orphanet:99844) |
MYELOPROLIFERATIVE SYNDROME, TRANSIENT | (OMIM:159595) |
Majeed syndrome | (Orphanet:77297) |
Mevalonic aciduria | (Orphanet:29) |
Muckle-Wells syndrome | (Orphanet:575) |
Omenn syndrome | (Orphanet:39041) |
Polyarteritis nodosa | (Orphanet:767) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Polycythemia vera | (Orphanet:729) |
Pyomyositis | (Orphanet:764) |
Schnitzler syndrome | (Orphanet:37748) |
Sweet syndrome | (Orphanet:3243) |
Systemic capillary leak syndrome | (Orphanet:188) |
TRAPS syndrome | (Orphanet:32960) |