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Cerebelloparenchymal disorder 3
Other Names for this Disease
- Autosomal recessive cerebelloparenchymal disorder type 3
- Cerebellar granular cell hypoplasia and mental retardation, congenital
- Cerebellar hypoplasia, nonprogressive Norman type
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Clinical Trials & Research for this Disease
- The Centers for Mendelian Genomics program is working to discover the causes of rare genetic disorders. For more information about applying to the research study, please visit their website.