Congenital factor xi deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CONGENITAL FACTOR XI DEFICIENCY
329MONDO:0012897
F11 Unknown
15026311 15180874 15566468 15953011 18312365 21649796 22159456 2813350 3286010 9518045
ClinGen, Orphanet
All1 Causal0 Unknown1
Related Diseases Diseases that share the most curated genes with Congenital factor xi deficiency.
5 View disease cluster →
Factor xi deficiency 1 shared geneF11 Related via 1 shared gene including F11. Coagulation factor deficiency syndrome 1 shared geneF11 Related via 1 shared gene including F11. Intracranial thrombosis 1 shared geneF11 Related via 1 shared gene including F11. Thromboembolic pulmonary hypertension 1 shared geneF11 Related via 1 shared gene including F11. Cor pulmonale 1 shared geneF11 Related via 1 shared gene including F11.