Fanconi anemia complementation group o

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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
Fanco
MONDO_0013248
RAD51C Unknown
20400963
Open Targets
Fanconi anemia complementation group O
MONDO_0013248
RAD51C Causal
19686080 20400963 22232082 24141787 26681308 29278735 32048120 32086639 37031326
ClinGen, Open Targets
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Fanconi anemia complementation group o.
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Breast-ovarian cancer, familial, susceptibility to, 3 1 shared geneRAD51C Related via 1 shared gene including RAD51C. Familial ovarian cancer 1 shared geneRAD51C Related via 1 shared gene including RAD51C. Cancer predisposition 1 shared geneRAD51C Related via 1 shared gene including RAD51C. Hereditary breast and ovarian cancer syndrome 1 shared geneRAD51C Related via 1 shared gene including RAD51C. Hepatosplenic t-cell lymphoma 1 shared geneRAD51C Related via 1 shared gene including RAD51C.