immunodeficiency, developmental delay, and hypohomocysteinemia

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Immunodeficiency, developmental delay, and hypohomocysteinemia
NFE2L2 Causal
29018201
ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with immunodeficiency, developmental delay, and hypohomocysteinemia.
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Developmental delay with immunodeficiency syndrome 1 shared geneNFE2L2 Related via 1 shared gene including NFE2L2. Hepatic insufficiency 1 shared geneNFE2L2 Related via 1 shared gene including NFE2L2. Keratosis 1 shared geneNFE2L2 Related via 1 shared gene including NFE2L2. Vascular system injury 1 shared geneNFE2L2 Related via 1 shared gene including NFE2L2. Endocrine system disease 1 shared geneNFE2L2 Related via 1 shared gene including NFE2L2.