Decreased CSF homovanillic acid
Symptom Information:
Symptom ID: | HPO:0003785 | ||
Synonyms: |
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Quality: | |||
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) Decreased CSF homovanillic acid(HPO:0003785) MedDRA: |
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Database Frequency: | 7 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Aromatic L-amino acid decarboxylase deficiency | (Orphanet:35708) |
Autosomal dominant dopa-responsive dystonia | (Orphanet:98808) |
Autosomal recessive dopa-responsive dystonia | (Orphanet:101150) |
Dihydropteridine reductase deficiency | (Orphanet:226) |
Dopa-responsive dystonia due to sepiapterin reductase deficiency | (Orphanet:70594) |
GTP cyclohydrolase I deficiency | (Orphanet:2102) |
Pyridoxal phosphate-responsive seizures | (Orphanet:79096) |