Fanconi anemia complementation group i

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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
Fanci
MONDO_0012186
FANCI Unknown
17452773
Open Targets
Fanconi anemia complementation group I
MONDO_0012186
FANCI Causal
11239453 17412408 17452773 17460694 19686080 32048120 32086639
ClinGen, Open Targets
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Fanconi anemia complementation group i.
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Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis 1 shared geneFANCI Related via 1 shared gene including FANCI. Bone marrow failure 1 shared geneFANCI Related via 1 shared gene including FANCI. Mitochondrial dna depletion syndrome 1 shared geneFANCI Related via 1 shared gene including FANCI. Fanconi anemia 1 shared geneFANCI Related via 1 shared gene including FANCI. Hereditary spastic paraplegia 1 shared geneFANCI Related via 1 shared gene including FANCI.