Congenital factor x deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CONGENITAL FACTOR X DEFICIENCY
328MONDO:0009212
F10 Unknown
15892863 26222694 26309706
ClinGen, GenCC, Orphanet
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Congenital factor x deficiency.
5 View disease cluster →
Factor x deficiency 1 shared geneF10 Related via 1 shared gene including F10. Blood coagulation disorder 1 shared geneF10 Related via 1 shared gene including F10. Thrombosis 1 shared geneF10 Related via 1 shared gene including F10. Psoriatic arthritis 1 shared geneF10 Related via 1 shared gene including F10. Preeclampsia 1 shared geneF10 Related via 1 shared gene including F10.