Cerebellar atrophy, mild
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 30 | (Orphanet:101010) |
Bilateral generalized polymicrogyria | (Orphanet:208447) |
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE | (OMIM:300861) |
Spinocerebellar ataxia type 3 | (Orphanet:98757) |