Human Phenotype Ontology 
Parent Node:
expand
Abnormality of the cerebrospinal fluid (HP:0002921)help
..Starting node
..expand
CSF pleocytosis (HP:0012229)help
Term ID:12229
Name:CSF pleocytosis
Definition:An increased white blood cell count in the cerebrospinal fluid.
Comments:
Reference:HP:0012229
MSeqDR-LSDB(LS)
& Disease (OMIM):
1.      OMIM: #603553 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, F..
2.      OMIM: %267700 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, F..
3.      (Child):HP:0200149- OMIM: #610329 AICARDI-GOUTIERES SYND..
4.      (Child):HP:0200149- OMIM: #610333 AICARDI-GOUTIERES SYND..
5.      (Child):HP:0009704- OMIM: #225750 AICARDI-GOUTIERES SYND..
6.      (Child):HP:0009704- OMIM: #610181 AICARDI-GOUTIERES SYND..
                  super
       Child Nodes:
........expandCSF lymphocytic pleiocytosis (HP:0200149) help
........expandCSF polymorphonuclear pleocytosis (HP:0012756) help

 Sister Nodes: 
..expandAbnormal CSF biopterin level (HP:0040207) help
..expandAbnormal CSF dopamine level (HP:0012654) help
..expandAbnormal CSF lactate level (HP:0030085) help
..expandAbnormal CSF neopterin level (HP:0040203) help
..expandDecreased CSF homovanillic acid (HVA) (HP:0003785) help
..expandExtra-axial cerebrospinal fluid accumulation (HP:0012510) help
..expandHydrocephalus (HP:0000238) help
..expandHypoglycorrhachia (HP:0011972) help
..expandIncreased CSF interferon alpha (HP:0009709) help
..expandIncreased CSF protein (HP:0002922) help
..expandLow CSF 5-methyltetrahydrofolate (HP:0012446) help
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium.