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eRAM

encyclopedia of Rare Disease Annotation for Precision Medicine




Disease congenital disorders of glycosylation
Comorbidity C0007758|cerebellar ataxia
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PubMedID- 25425520 In group 1, five patients had a medical history: cerebellar ataxia due to congenital disorder of glycosylation (cdg) 1 in three cases, mitochondrial disease in one case, and autoimmune deficiencies in one case.

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