Human Phenotype Ontology 
Parent Node:
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Abnormality of the cerebrospinal fluid (HP:0002921)help
..Starting node
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Increased CSF protein (HP:0002922)help
Term ID:2922
Name:Increased CSF protein
Definition:Increased concentration of protein in the cerebrospinal fluid.
Comments:
Reference:HP:0002922
MSeqDR-LSDB(LS)
& Disease (OMIM):
1. LS OMIM: #203700 MITOCHONDRIAL DNA DEPLETION SYNDROME ..
2. LS OMIM: #258450 PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA ..
3. LS OMIM: KEARNS-SAYRE SYNDROME..
4.      OMIM: #105210 AMYLOIDOSIS, HEREDITARY, TRANSTHYRETI..
5.      OMIM: #145900 HYPERTROPHIC NEUROPATHY OF DEJERINE-S..
6.      OMIM: #218000 AGENESIS OF THE CORPUS CALLOSUM WITH ..
7.      OMIM: #245200 KRABBE DISEASE;;GLOBOID CELL LEUKODYS..
8.      OMIM: #250100 METACHROMATIC LEUKODYSTROPHY;;MLD;;ME..
9.      OMIM: #251290 BAND-LIKE CALCIFICATION WITH SIMPLIFI..
10.      OMIM: #272200 MULTIPLE SULFATASE DEFICIENCY; MSD;;M..
11.      OMIM: #603553 HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, F..

Warning: 10 out of 22 matches reported due to space limit
                  super
       Child Nodes:

 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
..expandCSF pleocytosis (HP:0012229) 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
..expandLow CSF 5-methyltetrahydrofolate (HP:0012446) help
 

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