Increased CSF protein
Symptom Information:
Symptom ID: | HPO:0002922 | ||||||||||||||||
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 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) |
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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) |