L-ferritin deficiency

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
L-ferritin deficiency
MONDO_0014274
FTL Causal
23940258
Open Targets
L-ferritin deficiency, dominant and recessive
MONDO_0014274
FTL Unknown
23940258 18413574 23421845 19176363
Open Targets
All1 Causal1 Unknown1
Related Diseases Diseases that share the most curated genes with L-ferritin deficiency.
5 View disease cluster →
Genetic hyperferritinemia without iron overload 1 shared geneFTL Related via 1 shared gene including FTL. Hereditary hyperferritinemia with congenital cataracts 1 shared geneFTL Related via 1 shared gene including FTL. Neuroferritinopathy 1 shared geneFTL Related via 1 shared gene including FTL. Hyperferritinemia with or without cataract 1 shared geneFTL Related via 1 shared gene including FTL. Hyperferritinemia 1 shared geneFTL Related via 1 shared gene including FTL.