Brainstem atrophy
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Database Frequency: | 5 / 7739 | |
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All diseases associated with this symptom:
Autosomal recessive spastic paraplegia type 35 | (Orphanet:171629) |
Combined oxidative phosphorylation defect type 14 | (Orphanet:319519) |
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 5 | (OMIM:613477) |
Infantile onset spinocerebellar ataxia | (Orphanet:1186) |
Pontocerebellar hypoplasia type 6 | (Orphanet:166073) |