Ataxia with vitamin E deficiency Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Ataxia with vitamin E deficiency (AVED) is a neurodegenerative disease belonging to the inherited cerebellar ataxias. It is mainly characterized by progressive spino-cerebellar ataxia, loss of proprioception, areflexia, and is associated with a marked deficiency in vitamin E. (Orphanet Rare Disease Ontology, Orphanet_96)
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3 genes/proteins associated with the disease Ataxia with vitamin E deficiency from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
APOB apolipoprotein B 2.88009
APOA1 apolipoprotein A-I 2.88009
TTPA tocopherol (alpha) transfer protein 2.88009