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
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with Fanconi anemia complementation group i.
5 View disease cluster →
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.