Congenital thrombotic thrombocytopenic purpura

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CONGENITAL THROMBOTIC DISEASE, DUE TO PROTEIN C DEFICIENCY
C2930896MESH:C535424
PROC Unknown
25748729
CTD, Disgenet
CONGENITAL THROMBOTIC THROMBOCYTOPENIC PURPURA
93583C1268935MONDO:0010122
ADAMTS13 Unknown
11586351 12393505 12775718 17003922 19055667 22529289 25587650 28254814
ClinGen, Disgenet, Orphanet
All2 Causal0 Unknown2
Related Diseases Diseases that share the most curated genes with Congenital thrombotic thrombocytopenic purpura.
5 View disease cluster →
Central retinal vein occlusion 1 shared genePROC Related via 1 shared gene including PROC. hereditary thrombophilia due to congenital protein C deficiency 1 shared genePROC Related via 1 shared gene including PROC. Upshaw-schulman syndrome 1 shared geneADAMTS13 Related via 1 shared gene including ADAMTS13. Three-vessel coronary artery disease 1 shared geneADAMTS13 Related via 1 shared gene including ADAMTS13. Arteritis 1 shared genePROC Related via 1 shared gene including PROC.