CSF pleocytosis
Symptom Information:
Symptom ID: | HPO:0012229 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system morphology(HPO:0012639) Morphological abnormality of the central nervous system(HPO:0002011) Abnormality of the cerebrospinal fluid(HPO:0002921) CSF pleocytosis(HPO:0012229) MedDRA: |
||||
Database Frequency: | 5 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Familial hemophagocytic lymphohistiocytosis | (Orphanet:540) |
Gaucher disease type 2 | (Orphanet:77260) |
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 | (OMIM:603553) |
Kawasaki disease | (Orphanet:2331) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |