Increased CSF protein

Symptom Information:

Symptom ID: HPO:0002922
Synonyms:
Cerebrospinal fluid protein increased [HPO:0002922]
Cerebrospinal fluid with increased protein [HPO:0002922]
Elevated cerebrospinal fluid protein [HPO:0002922]
Elevated csf protein [HPO:0002922]
Increased protein in csf [HPO:0002922]
Spinal fluid protein elevated [HPO:0002922]
Elevated CSF protein [OMIM:Elevated CSF protein]
Elevated cerebrospinal fluid protein [OMIM:Elevated cerebrospinal fluid protein]
Increased CSF protein [OMIM:Increased CSF protein]
Increased protein in CSF [OMIM:Increased protein in CSF]
Spinal fluid protein elevated [OMIM:Spinal fluid protein elevated]
CSF protein increased [OMIM:CSF protein increased]
Cerebrospinal fluid (CSF) with increased protein [OMIM:Cerebrospinal fluid (CSF) with increased protein]
Elevated cerebrospinal fluid (CSF) protein [OMIM:Elevated cerebrospinal fluid (CSF) protein]
Increased cerebrospinal fluid (CSF) protein (>100mg/dl) [OMIM:Increased cerebrospinal fluid (CSF) protein (>100mg/dl)]
CSF protein increased [MedDRA:10011575]
Quality:
Cross references:
OMIM: "Elevated CSF protein" [OMIM:Elevated CSF protein]
OMIM: "Elevated cerebrospinal fluid protein" [OMIM:Elevated cerebrospinal fluid protein]
OMIM: "Increased CSF protein" [OMIM:Increased CSF protein]
OMIM: "Increased protein in CSF" [OMIM:Increased protein in CSF]
OMIM: "Spinal fluid protein elevated" [OMIM:Spinal fluid protein elevated]
OMIM: "CSF protein increased" [OMIM:CSF protein increased]
OMIM: "Cerebrospinal fluid (CSF) with increased protein" [OMIM:Cerebrospinal fluid (CSF) with increased protein]
OMIM: "Elevated cerebrospinal fluid (CSF) protein" [OMIM:Elevated cerebrospinal fluid (CSF) protein]
OMIM: "Increased cerebrospinal fluid (CSF) protein (>100mg/dl)" [OMIM:Increased cerebrospinal fluid (CSF) protein (>100mg/dl)]
Is a (Direct Parents):
MedDRA Cerebrospinal fluid tests (excl microbiology)
HPO         Abnormality of the cerebrospinal fluid
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)
                   Increased CSF protein(HPO:0002922)
MedDRA:
Investigations(MedDRA:10022891)
    Neurological, special senses and psychiatric investigations(MedDRA:10029295)
       Cerebrospinal fluid tests (excl microbiology)(MedDRA:10008183)
          Increased CSF protein(HPO:0002922)
Database Frequency: 27 / 7739
Resource:

All diseases associated with this symptom:

ATTRV122I amyloidosis (Orphanet:85451)
Alexander disease (Orphanet:58)
Alpers syndrome (Orphanet:726)
Autosomal recessive progressive external ophthalmoplegia (Orphanet:254886)
CHOROID PLEXUS CALCIFICATION AND MENTAL RETARDATION (OMIM:215480)
Combined oxidative phosphorylation defect type 11 (Orphanet:324535)
Congenital intrauterine infection-like syndrome (Orphanet:1229)
Corpus callosum agenesis - neuronopathy (Orphanet:1496)
Creutzfeldt-Jakob disease (Orphanet:204)
DEAFNESS, SENSORINEURAL, WITH PERIPHERAL NEUROPATHY AND ARTERIAL DISEASE (OMIM:124950)
Dejerine-Sottas syndrome (Orphanet:64748)
Familial acute necrotizing encephalopathy (Orphanet:88619)
Familial amyloid polyneuropathy (Orphanet:85447)
Familial hemophagocytic lymphohistiocytosis (Orphanet:540)
Flynn-Aird syndrome (Orphanet:2047)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 1 (OMIM:267700)
HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 2 (OMIM:603553)
HYPERTROPHIC NEUROPATHY AND CATARACT (OMIM:239900)
KRABBE DISEASE (OMIM:245200)
KRABBE DISEASE, ATYPICAL, DUE TO SAPOSIN A DEFICIENCY (OMIM:611722)
Kearns-Sayre syndrome (Orphanet:480)
Krabbe disease (Orphanet:487)
METACHROMATIC LEUKODYSTROPHY (OMIM:250100)
Multiple sulfatase deficiency (Orphanet:585)
Primary CD59 deficiency (Orphanet:169464)
Refsum disease (Orphanet:773)
Sneddon syndrome (Orphanet:820)