Facial myokymia
Symptom Information:
Symptom ID: | HPO:0000317 | ||||
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 musculature(HPO:0003011) Abnormality of facial musculature(HPO:0000301) Facial myokymia(HPO:0000317) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of movement(HPO:0100022) Myokymia(HPO:0002411) Facial myokymia(HPO:0000317) Abnormality of head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Abnormality of facial soft tissue(HPO:0011799) Abnormality of facial musculature(HPO:0000301) Facial myokymia(HPO:0000317) MedDRA: |
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Database Frequency: | 5 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Familial dyskinesia and facial myokymia | (Orphanet:324588) |
Spinocerebellar ataxia type 12 | (Orphanet:98762) |
Spinocerebellar ataxia type 14 | (Orphanet:98763) |
Spinocerebellar ataxia type 25 | (Orphanet:101111) |
Spinocerebellar ataxia type 5 | (Orphanet:98766) |