Vitamin E, Familial Isolated Deficiency of

Nume		Vitamin E, Familial Isolated Deficiency of
Pagina Web		www.malacards.org
Clasificare globală Malacards		Boli genetice; Boli metabolice; Boli rare
Clasificari ICD10		Deficiency of vitamin E; Early-onset cerebellar ataxia
Clasificare anatomică Malacards		Boli ale ochiului; Boli neuronale

Boli A-Z		Abetalipoproteinemia Aceruloplasminemia Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Apraxia Arthrochalasia Ehlers-Danlos Syndrome Ataxia and Polyneuropathy, Adult-Onset Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia Ataxia-Oculomotor Apraxia 3 Ataxia with Vitamin E Deficiency Atherosclerosis Susceptibility Autosomal Recessive Cerebellar Ataxia Autosomal Recessive Disease Blood Group--Ahonen Cerebellar Disease Chylomicron Retention Disease Dysbaric Osteonecrosis Ehlers-Danlos Syndrome, Vascular Type Friedreich Ataxia 1 Hepatic Adenomas, Familial Hereditary Ataxia Hyperalphalipoproteinemia 1 Hypercholesterolemia, Familial Hyperlipidemia, Familial Combined Hyperlipoproteinemia, Type Iii Hyperlipoproteinemia, Type Iv Hypertriglyceridemia, Familial Hypoalphalipoproteinemia, Primary Hypobetalipoproteinemia, Familial, 1 Hypolipoproteinemia Leukodystrophy, Hypomyelinating, 3 Persistent Idiopathic Facial Pain Primary Cerebellar Degeneration Refsum Disease, Classic Retinitis Retinitis Pigmentosa Spastic Ataxia, Charlevoix-Saguenay Type Spinocerebellar Ataxia, Autosomal Recessive 1 Spinocerebellar Degeneration Tangier Disease Vitamin Metabolic Disorder