Pontocerebellar atrophy
Symptom Information:
Symptom ID: | HPO:0006879 | ||
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MedDRA: |
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Database Frequency: | 6 / 7739 | ||
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All diseases associated with this symptom:
DPM1-CDG | (Orphanet:79322) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
SPINOCEREBELLAR ATAXIA 40 | (OMIM:616053) |
SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 1 | (OMIM:606002) |
Spinocerebellar ataxia with axonal neuropathy type 2 | (Orphanet:64753) |
Wolfram syndrome 1 | (OMIM:222300) |