Chin myoclonus
Symptom Information:
Symptom ID: | HPO:0012462 | |||
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 musculature(HPO:0003011) Abnormality of muscle physiology(HPO:0011804) Involuntary movements(HPO:0004305) Myoclonus(HPO:0001336) Chin myoclonus(HPO:0012462) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of movement(HPO:0100022) Involuntary movements(HPO:0004305) Myoclonus(HPO:0001336) Chin myoclonus(HPO:0012462) MedDRA: |
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Database Frequency: | 1 / 7739 | |||
Resource: |
All diseases associated with this symptom:
Hereditary geniospasm | (Orphanet:53372) |