Vitamin e deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
FAMILIAL ISOLATED DEFICIENCY OF VITAMIN E
MONDO:0010188
TTPA Causal — ClinVar, GenCC
VITAMIN E DEFICIENCY
C0042875MESH:D014811
TTPA Unknown
11095717
CTD, Disgenet
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Vitamin e deficiency.
5 View disease cluster →
Ataxia with vitamin e deficiency 1 shared geneTTPA Related via 1 shared gene including TTPA. Urination disorders 1 shared geneTTPA Related via 1 shared gene including TTPA. Headache 1 shared geneTTPA Related via 1 shared gene including TTPA. Visual disorder 1 shared geneTTPA Related via 1 shared gene including TTPA. Nervous system disease 1 shared geneTTPA Related via 1 shared gene including TTPA.