Abnormality of the cerebrospinal fluid
Symptom Information:
Symptom ID: | HPO:0002921 | ||||||||
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) MedDRA: |
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Database Frequency: | 6 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
6-pyruvoyl-tetrahydropterin synthase deficiency | (Orphanet:13) |
Argininemia | (Orphanet:90) |
Autosomal dominant dopa-responsive dystonia | (Orphanet:98808) |
Dihydropteridine reductase deficiency | (Orphanet:226) |
Dopa-responsive dystonia due to sepiapterin reductase deficiency | (Orphanet:70594) |
GTP cyclohydrolase I deficiency | (Orphanet:2102) |