Hyperkinetic movements
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Database Frequency: | 4 / 7739 | |
Resource: |
All diseases associated with this symptom:
Autosomal recessive limb-girdle muscular dystrophy type 2S | (Orphanet:369840) |
Christianson syndrome | (Orphanet:85278) |
Encephalopathy due to prosaposin deficiency | (Orphanet:139406) |
Mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria | (Orphanet:1933) |