Fanconi anemia complementation group b

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Subtype of: Fanconi anemia
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Fanconi anemia complementation group B
MONDO_0019391
FANCB Causal
15502827 16679491 21910217 24416387 26683739 29232005 32048120 32086639
ClinGen, Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Fanconi anemia complementation group b.
5 View disease cluster →
Vacterl-hydrocephalus syndrome 1 shared geneFANCB Related via 1 shared gene including FANCB. Vacterl association, x-linked, with or without hydrocephalus 1 shared geneFANCB Related via 1 shared gene including FANCB. Vacterl association 1 shared geneFANCB Related via 1 shared gene including FANCB. Anorectal malformation 1 shared geneFANCB Related via 1 shared gene including FANCB. Bone marrow failure 1 shared geneFANCB Related via 1 shared gene including FANCB.