Loss of motor function
Symptom Information:
Symptom ID: | OMIM : No Id available | ||
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HPO:
MedDRA: |
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Database Frequency: | 3 / 7739 | ||
Resource: |
All diseases associated with this symptom:
CLN10 disease | (Orphanet:228337) |
Congenital neuronal ceroid lipofuscinosis | (Orphanet:168486) |
Progressive myoclonic epilepsy type 3 | (Orphanet:263516) |