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Hyperferritinemia with or without cataract
Hyperferritinemia with or without cataract
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Subtype of:
Hyperferritinemia
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Show by gene
(one row per gene, with all of its disease terms together)
Pathways column key:
KEGG
Reactome
Disease Term
Disease ID
Gene Symbol
Classification
References
Source
Pathways
Hyperferritinemia with or without cataract
MONDO_0010952
FTL
Unknown
19176363
Open Targets
Porphyrin metabolism
Ferroptosis
Necroptosis
Mineral absorption
Golgi Associated Vesicle Biogenesis
Neutrophil degranulation
Iron uptake and transport
+4 more
Hyperferritinemia-cataract syndrome OIMM
MONDO_0010952
FTL
Unknown
23940258
18413574
23421845
19176363
Open Targets
Porphyrin metabolism
Ferroptosis
Necroptosis
Mineral absorption
Golgi Associated Vesicle Biogenesis
Neutrophil degranulation
Iron uptake and transport
+4 more
All
1
Causal
0
Unknown
1
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Clear
ClinVar
0
Orphanet
0
Disgenet
0
CTD
0
HPO
0
GWAS catalog
0
GenCC
0
ClinGen
0
Open Targets
1
Related Diseases
Diseases that share the most curated genes with Hyperferritinemia with or without cataract.
5
View disease cluster →
Genetic hyperferritinemia without iron overload
1 shared gene
FTL
Related via 1 shared gene including FTL.
Hereditary hyperferritinemia with congenital cataracts
1 shared gene
FTL
Related via 1 shared gene including FTL.
Neuroferritinopathy
1 shared gene
FTL
Related via 1 shared gene including FTL.
L-ferritin deficiency
1 shared gene
FTL
Related via 1 shared gene including FTL.
Hyperferritinemia
1 shared gene
FTL
Related via 1 shared gene including FTL.
1
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