Parkinsonism with favorable response to dopaminergic medication
Symptom Information:
Symptom ID: | HPO:0002548 | ||
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 physiology(HPO:0012638) Abnormality of central motor function(HPO:0011442) Abnormality of extrapyramidal motor function(HPO:0002071) Parkinsonism(HPO:0001300) Parkinsonism with favorable response to dopaminergic medication(HPO:0002548) MedDRA: |
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Database Frequency: | 13 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant dopa-responsive dystonia | (Orphanet:98808) |
Autosomal dominant progressive external ophthalmoplegia | (Orphanet:254892) |
Autosomal recessive dopa-responsive dystonia | (Orphanet:101150) |
Benign paroxysmal tonic upgaze of childhood with ataxia | (Orphanet:1179) |
Dopa-responsive dystonia due to sepiapterin reductase deficiency | (Orphanet:70594) |
GTP cyclohydrolase I deficiency | (Orphanet:2102) |
Kufor-Rakeb syndrome | (Orphanet:306674) |
PARKINSON DISEASE 11, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO | (OMIM:607688) |
PARKINSON DISEASE 13, AUTOSOMAL DOMINANT, SUSCEPTIBILITY TO | (OMIM:610297) |
PARKINSON DISEASE 15, AUTOSOMAL RECESSIVE EARLY-ONSET | (OMIM:260300) |
PARKINSON DISEASE 8, AUTOSOMAL DOMINANT | (OMIM:607060) |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS,AUTOSOMAL DOMINANT, 1 | (OMIM:157640) |
X-linked dystonia-parkinsonism | (Orphanet:53351) |