Hemophilia b

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
HEMOPHILIA B
C0008533306900MESH:D002836MONDO:0010604
F2 Unknown — Disgenet
F9 Unknown
16643212 2388855 7062952 25330515 26612714 26964564 30210749 3286010 3416069 9639513
CTD, ClinGen, Disgenet, GWAS catalog, HPO
MILD HEMOPHILIA B
169799MONDO:0015717
F9 Unknown — GenCC, Orphanet
MODERATE HEMOPHILIA B
169796
F9 Unknown — Orphanet
MODERATELY SEVERE HEMOPHILIA B
MONDO:0015716
F9 Unknown
9169594 25470321 9600455 8680410 8257988 1902289 2738071 2713493 12588353 7981722 12604421 2162822 10094553 6603618 2472424 9222764 25251685 11122099 2773937 2775660 2339358 10698280 2753873 1346975 2592373 2372509 3243764 8199596 3790720 9452115 8295821
GenCC, ClinGen
All2 Causal0 Unknown2
Related Diseases Diseases that share the most curated genes with Hemophilia b.
5 View disease cluster →
Congenital factor ii deficiency 1 shared geneF2 Related via 1 shared gene including F2. Congenital prothrombin deficiency 1 shared geneF2 Related via 1 shared gene including F2. thrombophilia due to thrombin defect 1 shared geneF2 Related via 1 shared gene including F2. Hemophilia b carriers 1 shared geneF9 Related via 1 shared gene including F9. thrombophilia, X-linked, due to factor 9 defect 1 shared geneF9 Related via 1 shared gene including F9.