Progressive extrapyramidal movement disorder
Symptom Information:
Symptom ID: | HPO:0007153 | ||
Synonyms: |
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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) Progressive extrapyramidal movement disorder(HPO:0007153) MedDRA: |
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Database Frequency: | 1 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Guanidinoacetate methyltransferase deficiency | (Orphanet:382) |