Rh deficiency syndrome

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
RH DEFICIENCY SYNDROME
71275C0272052MONDO:0019107
RHAG Causal
8563755 9716608
Disgenet, GenCC, Orphanet
RHCE Unknown
9657766 9657769
Disgenet, GWAS catalog, Orphanet
RHD Unknown
9657769
Disgenet, GWAS catalog, Orphanet
All3 Causal1 Unknown2
Related Diseases Diseases that share the most curated genes with Rh deficiency syndrome.
5 View disease cluster →
Rh-null, regulator type 1 shared geneRHAG Related via 1 shared gene including RHAG. Rh-null, amorph type 1 shared geneRHCE Related via 1 shared gene including RHCE. Alpha-1 antichymotrypsin deficiency 1 shared geneRHD Related via 1 shared gene including RHD. Hemolytic disease of fetus and newborn 1 shared geneRHD Related via 1 shared gene including RHD. Rh isoimmunization 1 shared geneRHD Related via 1 shared gene including RHD.