Congenital factor xiii deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CONGENITAL FACTOR XIII DEFICIENCY
331MONDO:0018029
F13A1 Unknown
21738029
GWAS catalog, Orphanet
F13B Unknown
21738029
CTD, Orphanet
All2 Causal0 Unknown2
Related Diseases Diseases that share the most curated genes with Congenital factor xiii deficiency.
5 View disease cluster →
Factor xiii deficiency 2 shared genesF13A1, F13B Related via 2 shared genes including F13A1, F13B. Coagulation factor deficiency syndrome 1 shared geneF13B Related via 1 shared gene including F13B. Cholesteatoma 1 shared geneF13B Related via 1 shared gene including F13B. Disseminated intravascular coagulation 1 shared geneF13A1 Related via 1 shared gene including F13A1. Venous thrombosis 2 shared genesF13A1, F13B Related via 2 shared genes including F13A1, F13B.