Craniofacial dystonia
Symptom Information:
| Symptom ID: | HPO:0012179 | ||
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HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system physiology(HPO:0012638) Abnormality of movement(HPO:0100022) Dystonia(HPO:0001332) Focal dystonia(HPO:0004373) Craniofacial dystonia(HPO:0012179) MedDRA: |
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| Database Frequency: | 4 / 7739 | ||
| Resource: |
All diseases associated with this symptom:
| Autosomal dominant spastic paraplegia type 6 | (Orphanet:100988) |
| DYSTONIA WITH CEREBELLAR ATROPHY | (OMIM:611694) |
| Mohr-Tranebjaerg syndrome | (Orphanet:52368) |
| Thiamine-responsive encephalopathy | (Orphanet:199348) |