Factor x deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
FACTOR X DEFICIENCY
227600C0015519MESH:D005171
F10 Causal
15075089 12574802 10739379 15650540 7669671 26222694 10746568 1973167 7860069 12945883 11728527 25313940 8910490 8845463 11248282 19135706 1985698 2790181 8529633 17393015 10468877
CTD, Disgenet, HPO
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Factor x deficiency.
5 View disease cluster →
Congenital 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.