has material basis in germline mutation in TTPA inborn vitamin metabolic disorder familial isolated deficiency of vitamin E https://www.malacards.org/card/ataxia_with_vitamin_e_deficiency MEDGEN:341248 OMIM:277460 VED NANDO:1200050 ICD9:269.1 MedDRA:10047631 MESH:C535393 NORD:817 DOID:0090028 GARD:0008595 familial isolated deficiency of vitamin type E Orphanet:96 UMLS:C1848533 ataxia, Friedreich-like, with selective vitamin E deficiency MONDO:0010188 ataxia with vitamin E deficiency ICD9:334.3 isolated vitamin E deficiency Friedreich-like ataxia Friedreich-like ataxia with selective vitamin E deficiency SCTID:702442008 familial isolated vitamin E deficiency Ataxia with Vitamin E Deficiency 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. ataxia with isolated vitamin E deficiency AVED vitamin E, familial isolated deficiency OF autosomal recessive metabolic cerebellar ataxia hereditary peripheral neuropathy