Upper limb involvement
Symptom Information:
Symptom ID: | OMIM : No Id available | |||
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Database Frequency: | 4 / 7739 | |||
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All diseases associated with this symptom:
Autosomal recessive spastic paraplegia type 26 | (Orphanet:101006) |
Infantile-onset ascending hereditary spastic paralysis | (Orphanet:293168) |
Spastic paraplegia type 2 | (Orphanet:99015) |
Spinocerebellar ataxia type 25 | (Orphanet:101111) |