Cortisone reductase deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CORTISONE REDUCTASE DEFICIENCY
C1291245MESH:C536447MONDO:0000193
H6PD Unknown
18628520
CTD, Disgenet, Orphanet
HSD11B1 Unknown
21325058 25526675
CTD, Disgenet, GWAS catalog
All2 Causal2 Unknown2
Related Diseases Diseases that share the most curated genes with Cortisone reductase deficiency.
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Hyperandrogenism 2 shared genesHSD11B1, H6PD Related via 2 shared genes including HSD11B1, H6PD. Omphalocele exstrophy imperforate anus 1 shared geneHSD11B1 Related via 1 shared gene including HSD11B1. Hyperglycemia 1 shared geneHSD11B1 Related via 1 shared gene including HSD11B1. Allergic contact dermatitis 1 shared geneHSD11B1 Related via 1 shared gene including HSD11B1. Venous thromboembolism 1 shared geneH6PD Related via 1 shared gene including H6PD.