Familial isolated vitamin e deficiency
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| Familial isolated vitamin e deficiency Classification and external resources |
|
| ICD-10 | GroupMajor.minor |
|---|---|
| ICD-9 | xxx |
| OMIM | 277460 600415 |
| DiseasesDB | 30633 |
Familial Isolated Vitamin E Deficiency is a rare, autosomal recessive neurodegenerative disease. Symptoms are similar to those of Friedreich ataxia.
[edit] Cause
Familial Isolated Vitamin E Deficiency is caused by mutations in the gene for a-tocopherol transfer protein.

