Combined deficiency of vitamin k-dependent clotting factors

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 1
277450C1848534MESH:C564741
GGCX Unknown — CTD, Disgenet, HPO
MAT2A Unknown — Disgenet
VKORC1 Unknown — Disgenet
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, 2
607473C1843832OMIM:607473
VKORC1 Unknown
14765194
CTD, Disgenet, HPO
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, TYPE 1
MONDO:0010187
GGCX Causal
15287948 16720838 17110937 17327402 19116367 24520408 25151188 2617472 26758921 29175035 9166845 9845520
ClinGen, ClinVar, GWAS catalog
VKORC1 Unknown
14765194
CTD
VITAMIN K-DEPENDENT CLOTTING FACTORS, COMBINED DEFICIENCY OF, TYPE 2
MONDO:0011837
VKORC1 Causal
14765194 18315553 19492146 31353023
ClinGen, ClinVar, Disgenet
All3 Causal2 Unknown3
Related Diseases Diseases that share the most curated genes with Combined deficiency of vitamin k-dependent clotting factors.
5 View disease cluster →
Body skin hyperlaxity 1 shared geneGGCX Related via 1 shared gene including GGCX. Coumarin resistance 1 shared geneVKORC1 Related via 1 shared gene including VKORC1. Aortic rupture 1 shared geneVKORC1 Related via 1 shared gene including VKORC1. Blood coagulation disorder 2 shared genesVKORC1, GGCX Related via 2 shared genes including VKORC1, GGCX. familial thoracic aortic aneurysm and aortic dissection 1 shared geneMAT2A Related via 1 shared gene including MAT2A.